ClinVar Miner

List of variants in gene ABCC2 reported as uncertain significance for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 201
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000392.5(ABCC2):c.2009T>C (p.Ile670Thr) rs17222632 0.00388
NM_000392.5(ABCC2):c.1032-3C>T rs139800035 0.00253
NM_000392.5(ABCC2):c.4430C>T (p.Thr1477Met) rs142573385 0.00173
NM_000392.5(ABCC2):c.3492C>T (p.Ser1164=) rs144192700 0.00159
NM_000392.5(ABCC2):c.3026T>C (p.Ile1009Thr) rs57351269 0.00129
NM_000392.5(ABCC2):c.998A>G (p.Asp333Gly) rs17222674 0.00120
NM_000392.5(ABCC2):c.3614+6G>C rs17222716 0.00103
NM_000392.5(ABCC2):c.258A>G (p.Val86=) rs142443276 0.00091
NM_000392.5(ABCC2):c.4495A>G (p.Met1499Val) rs149200446 0.00078
NM_000392.5(ABCC2):c.1860T>A (p.Asp620Glu) rs141413284 0.00075
NM_000392.5(ABCC2):c.4071G>C (p.Gln1357His) rs148393425 0.00062
NM_000392.5(ABCC2):c.3561G>A (p.Glu1187=) rs17216324 0.00059
NM_000392.5(ABCC2):c.3521G>A (p.Arg1174His) rs139188247 0.00057
NM_000392.5(ABCC2):c.2613A>G (p.Glu871=) rs76302654 0.00056
NM_000392.5(ABCC2):c.736A>C (p.Met246Leu) rs17222744 0.00051
NM_000392.5(ABCC2):c.3236G>A (p.Arg1079Gln) rs145672804 0.00044
NM_000392.5(ABCC2):c.4075A>C (p.Ile1359Leu) rs142700351 0.00044
NM_000392.5(ABCC2):c.3008G>T (p.Trp1003Leu) rs147566977 0.00040
NM_000392.5(ABCC2):c.1007C>T (p.Thr336Met) rs149854486 0.00039
NM_000392.5(ABCC2):c.3648C>A (p.Asn1216Lys) rs144967259 0.00038
NM_000392.5(ABCC2):c.1250T>C (p.Val417Ala) rs199595780 0.00036
NM_000392.5(ABCC2):c.2408T>C (p.Val803Ala) rs148835620 0.00036
NM_000392.5(ABCC2):c.339G>A (p.Leu113=) rs151304543 0.00032
NM_000392.5(ABCC2):c.3057G>C (p.Gln1019His) rs144521346 0.00026
NM_000392.5(ABCC2):c.3500T>C (p.Val1167Ala) rs140680467 0.00024
NM_000392.5(ABCC2):c.469-9T>C rs147614414 0.00024
NM_000392.5(ABCC2):c.1602G>T (p.Lys534Asn) rs149593061 0.00022
NM_000392.5(ABCC2):c.1696G>A (p.Val566Ile) rs145520251 0.00022
NM_000392.5(ABCC2):c.4348G>T (p.Ala1450Ser) rs56296335 0.00021
NM_000392.5(ABCC2):c.1950G>A (p.Ser650=) rs138673546 0.00019
NM_000392.5(ABCC2):c.2499T>C (p.Val833=) rs75148532 0.00019
NM_000392.5(ABCC2):c.2093A>G (p.Lys698Arg) rs199859869 0.00015
NM_000392.5(ABCC2):c.1585C>T (p.Arg529Trp) rs138799687 0.00012
NM_000392.5(ABCC2):c.3081C>T (p.Tyr1027=) rs201212360 0.00012
NM_000392.5(ABCC2):c.3436C>T (p.Arg1146Cys) rs377550597 0.00011
NM_000392.5(ABCC2):c.3888C>G (p.Ser1296Arg) rs143990242 0.00011
NM_000392.5(ABCC2):c.763C>T (p.Arg255Trp) rs147494662 0.00011
NM_000392.5(ABCC2):c.1457C>T (p.Thr486Ile) rs17222589 0.00010
NM_000392.5(ABCC2):c.3834G>A (p.Val1278=) rs150472537 0.00009
NM_000392.5(ABCC2):c.718A>G (p.Ser240Gly) rs750440697 0.00009
NM_000392.5(ABCC2):c.23C>T (p.Ser8Phe) rs375147383 0.00008
NM_000392.5(ABCC2):c.2461A>G (p.Ser821Gly) rs147649283 0.00007
NM_000392.5(ABCC2):c.3796A>G (p.Ile1266Val) rs148292402 0.00007
NM_000392.5(ABCC2):c.1178G>A (p.Arg393Gln) rs763509429 0.00006
NM_000392.5(ABCC2):c.2942T>C (p.Phe981Ser) rs767455559 0.00006
NM_000392.5(ABCC2):c.3082G>A (p.Gly1028Arg) rs148887680 0.00006
NM_000392.5(ABCC2):c.3437G>A (p.Arg1146His) rs148551677 0.00006
NM_000392.5(ABCC2):c.3499G>A (p.Val1167Ile) rs367739304 0.00006
NM_000392.5(ABCC2):c.3547C>A (p.Leu1183Met) rs145008610 0.00006
NM_000392.5(ABCC2):c.3576C>G (p.Thr1192=) rs146575217 0.00006
NM_000392.5(ABCC2):c.3615G>A (p.Arg1205=) rs377593832 0.00006
NM_000392.5(ABCC2):c.3987+10G>A rs373365135 0.00006
NM_000392.5(ABCC2):c.4507_4508+2del rs758461922 0.00006
NM_000392.5(ABCC2):c.655C>T (p.Arg219Cys) rs572309746 0.00006
NM_000392.5(ABCC2):c.232C>T (p.Leu78=) rs764390911 0.00005
NM_000392.5(ABCC2):c.4546G>A (p.Gly1516Ser) rs186295082 0.00005
NM_000392.5(ABCC2):c.1586G>A (p.Arg529Gln) rs781337846 0.00004
NM_000392.5(ABCC2):c.213C>T (p.Phe71=) rs770824435 0.00004
NM_000392.5(ABCC2):c.3011C>T (p.Thr1004Ile) rs775253982 0.00004
NM_000392.5(ABCC2):c.3591C>G (p.Val1197=) rs774159224 0.00004
NM_000392.5(ABCC2):c.4240C>T (p.His1414Tyr) rs544311254 0.00004
NM_000392.5(ABCC2):c.4314C>T (p.Ser1438=) rs376790802 0.00004
NM_000392.5(ABCC2):c.470G>T (p.Gly157Val) rs140550051 0.00004
NM_000392.5(ABCC2):c.517G>A (p.Gly173Arg) rs138663047 0.00004
NM_000392.5(ABCC2):c.577-3C>T rs370534491 0.00004
NM_000392.5(ABCC2):c.1769G>A (p.Arg590His) rs751940502 0.00003
NM_000392.5(ABCC2):c.1835G>A (p.Arg612Gln) rs376124211 0.00003
NM_000392.5(ABCC2):c.2911C>G (p.Leu971Val) rs772482844 0.00003
NM_000392.5(ABCC2):c.682G>A (p.Glu228Lys) rs774163715 0.00003
NM_000392.5(ABCC2):c.908A>G (p.Lys303Arg) rs200342237 0.00003
NM_000392.5(ABCC2):c.1109C>T (p.Ala370Val) rs144390464 0.00002
NM_000392.5(ABCC2):c.1319T>G (p.Met440Arg) rs996397410 0.00002
NM_000392.5(ABCC2):c.1658C>T (p.Thr553Ile) rs191954987 0.00002
NM_000392.5(ABCC2):c.2504G>A (p.Gly835Glu) rs369677401 0.00002
NM_000392.5(ABCC2):c.306C>A (p.Thr102=) rs559908064 0.00002
NM_000392.5(ABCC2):c.3690A>C (p.Arg1230Ser) rs753282654 0.00002
NM_000392.5(ABCC2):c.3927C>T (p.Tyr1309=) rs4148401 0.00002
NM_000392.5(ABCC2):c.3973G>A (p.Gly1325Ser) rs759452729 0.00002
NM_000392.5(ABCC2):c.4179G>T (p.Met1393Ile) rs779736415 0.00002
NM_000392.5(ABCC2):c.4357C>T (p.Arg1453Trp) rs769022665 0.00002
NM_000392.5(ABCC2):c.4431G>A (p.Thr1477=) rs146718433 0.00002
NM_000392.5(ABCC2):c.958A>G (p.Met320Val) rs375385616 0.00002
NM_000392.5(ABCC2):c.1051A>G (p.Ser351Gly) rs1288501345 0.00001
NM_000392.5(ABCC2):c.1183G>A (p.Ala395Thr) rs886042227 0.00001
NM_000392.5(ABCC2):c.1344T>G (p.Ile448Met) rs370095941 0.00001
NM_000392.5(ABCC2):c.1429A>C (p.Asn477His) rs1564677235 0.00001
NM_000392.5(ABCC2):c.1792A>G (p.Met598Val) rs1472006497 0.00001
NM_000392.5(ABCC2):c.1876G>T (p.Ala626Ser) rs765154081 0.00001
NM_000392.5(ABCC2):c.1964G>A (p.Arg655Gln) rs200976632 0.00001
NM_000392.5(ABCC2):c.2056G>A (p.Gly686Arg) rs1359163275 0.00001
NM_000392.5(ABCC2):c.2077G>A (p.Gly693Arg) rs765570396 0.00001
NM_000392.5(ABCC2):c.208G>A (p.Val70Ile) rs199700510 0.00001
NM_000392.5(ABCC2):c.2095-7C>T rs774902843 0.00001
NM_000392.5(ABCC2):c.2201T>C (p.Leu734Pro) rs745982246 0.00001
NM_000392.5(ABCC2):c.2303G>A (p.Arg768Gln) rs536840524 0.00001
NM_000392.5(ABCC2):c.2439+6A>C rs1564688760 0.00001
NM_000392.5(ABCC2):c.2588T>C (p.Leu863Pro) rs201820826 0.00001
NM_000392.5(ABCC2):c.2963T>A (p.Met988Lys) rs748479566 0.00001
NM_000392.5(ABCC2):c.3021T>C (p.Ser1007=) rs892786074 0.00001
NM_000392.5(ABCC2):c.330A>G (p.Thr110=) rs750755532 0.00001
NM_000392.5(ABCC2):c.3493G>A (p.Glu1165Lys) rs199938496 0.00001
NM_000392.5(ABCC2):c.3524C>T (p.Ala1175Val) rs1272618565 0.00001
NM_000392.5(ABCC2):c.3583A>G (p.Lys1195Glu) rs1235065840 0.00001
NM_000392.5(ABCC2):c.3752C>T (p.Thr1251Ile) rs750342363 0.00001
NM_000392.5(ABCC2):c.3772A>G (p.Met1258Val) rs768755574 0.00001
NM_000392.5(ABCC2):c.3873G>A (p.Pro1291=) rs765304225 0.00001
NM_000392.5(ABCC2):c.4039C>T (p.Leu1347Phe) rs767694433 0.00001
NM_000392.5(ABCC2):c.4220G>C (p.Trp1407Ser) rs1197522109 0.00001
NM_000392.5(ABCC2):c.4382A>G (p.Asp1461Gly) rs201658889 0.00001
NM_000392.5(ABCC2):c.4398G>A (p.Ala1466=) rs780515921 0.00001
NM_000392.5(ABCC2):c.4508+6T>C rs766426423 0.00001
NM_000392.5(ABCC2):c.4528G>A (p.Gly1510Arg) rs751985179 0.00001
NM_000392.5(ABCC2):c.650A>C (p.Tyr217Ser) rs202129492 0.00001
NM_000392.5(ABCC2):c.855T>C (p.Asp285=) rs769700101 0.00001
NM_000392.5(ABCC2):c.1007C>G (p.Thr336Arg) rs149854486
NM_000392.5(ABCC2):c.1034T>G (p.Leu345Trp)
NM_000392.5(ABCC2):c.1088G>A (p.Cys363Tyr) rs1564675319
NM_000392.5(ABCC2):c.1249_1250inv (p.Val417Thr)
NM_000392.5(ABCC2):c.1261G>A (p.Val421Met) rs1564676980
NM_000392.5(ABCC2):c.1321C>A (p.Leu441Met) rs374787164
NM_000392.5(ABCC2):c.1323G>A (p.Leu441=)
NM_000392.5(ABCC2):c.1408delinsTTGG (p.Met470delinsLeuVal) rs1564677201
NM_000392.5(ABCC2):c.1434G>A (p.Ala478=) rs4267009
NM_000392.5(ABCC2):c.1435A>G (p.Ile479Val)
NM_000392.5(ABCC2):c.1439T>C (p.Leu480Pro)
NM_000392.5(ABCC2):c.1446C>T (p.Thr482=) rs113646094
NM_000392.5(ABCC2):c.1464+4A>C rs753102845
NM_000392.5(ABCC2):c.1475T>C (p.Met492Thr)
NM_000392.5(ABCC2):c.1609C>A (p.Leu537Met)
NM_000392.5(ABCC2):c.1610T>C (p.Leu537Pro) rs1564679059
NM_000392.5(ABCC2):c.1644C>A (p.Phe548Leu)
NM_000392.5(ABCC2):c.1648T>G (p.Phe550Val)
NM_000392.5(ABCC2):c.1751C>A (p.Thr584Asn) rs1564679568
NM_000392.5(ABCC2):c.1866G>A (p.Leu622=)
NM_000392.5(ABCC2):c.1900+3A>C
NM_000392.5(ABCC2):c.1939G>C (p.Glu647Gln)
NM_000392.5(ABCC2):c.1981A>G (p.Ile661Val) rs1564682199
NM_000392.5(ABCC2):c.2034C>T (p.Ser678=) rs1554850241
NM_000392.5(ABCC2):c.2057G>A (p.Gly686Glu)
NM_000392.5(ABCC2):c.2139C>T (p.Gly713=) rs1564687797
NM_000392.5(ABCC2):c.2149_2151del (p.Asp717del) rs1198723210
NM_000392.5(ABCC2):c.2151C>A (p.Asp717Glu) rs1554851498
NM_000392.5(ABCC2):c.223CTT[1] (p.Leu76del)
NM_000392.5(ABCC2):c.2246G>T (p.Gly749Val)
NM_000392.5(ABCC2):c.2273G>T (p.Gly758Val) rs786205465
NM_000392.5(ABCC2):c.2303G>C (p.Arg768Pro) rs536840524
NM_000392.5(ABCC2):c.2306T>C (p.Ile769Thr) rs762655590
NM_000392.5(ABCC2):c.2343C>G (p.Ile781Met) rs1564688620
NM_000392.5(ABCC2):c.2352A>G (p.Leu784=) rs483352691
NM_000392.5(ABCC2):c.2367T>G (p.Ser789=) rs1564688688
NM_000392.5(ABCC2):c.2455A>G (p.Thr819Ala)
NM_000392.5(ABCC2):c.2472T>C (p.Phe824=) rs867615681
NM_000392.5(ABCC2):c.2620+10_2620+12del rs764566414
NM_000392.5(ABCC2):c.263C>A (p.Thr88Lys) rs1564669915
NM_000392.5(ABCC2):c.2922A>G (p.Ile974Met) rs184055071
NM_000392.5(ABCC2):c.2955G>A (p.Ala985=) rs139082536
NM_000392.5(ABCC2):c.3009G>C (p.Trp1003Cys) rs1564695476
NM_000392.5(ABCC2):c.3057G>A (p.Gln1019=) rs144521346
NM_000392.5(ABCC2):c.3148G>A (p.Val1050Ile)
NM_000392.5(ABCC2):c.3149T>C (p.Val1050Ala)
NM_000392.5(ABCC2):c.3258+2dup
NM_000392.5(ABCC2):c.334-3C>T
NM_000392.5(ABCC2):c.3424G>C (p.Val1142Leu) rs375280444
NM_000392.5(ABCC2):c.3442C>G (p.Leu1148Val) rs757405951
NM_000392.5(ABCC2):c.3498C>T (p.Thr1166=) rs564908429
NM_000392.5(ABCC2):c.3525C>G (p.Ala1175=) rs1554853606
NM_000392.5(ABCC2):c.3535C>G (p.Gln1179Glu)
NM_000392.5(ABCC2):c.3907A>C (p.Asn1303His)
NM_000392.5(ABCC2):c.3944T>G (p.Leu1315Arg) rs1554854276
NM_000392.5(ABCC2):c.400C>T (p.Leu134=) rs1564670755
NM_000392.5(ABCC2):c.4027C>T (p.Leu1343Phe)
NM_000392.5(ABCC2):c.4046G>C (p.Arg1349Thr) rs756482190
NM_000392.5(ABCC2):c.4079T>C (p.Ile1360Thr) rs780758213
NM_000392.5(ABCC2):c.4088T>C (p.Val1363Ala)
NM_000392.5(ABCC2):c.4103T>C (p.Ile1368Thr)
NM_000392.5(ABCC2):c.4108C>T (p.Leu1370Phe)
NM_000392.5(ABCC2):c.4159T>C (p.Phe1387Leu) rs1564702291
NM_000392.5(ABCC2):c.4160T>C (p.Phe1387Ser) rs1554854589
NM_000392.5(ABCC2):c.4175_4180del (p.Arg1392_Met1393del) rs749662916
NM_000392.5(ABCC2):c.417G>T (p.Ser139=) rs145350474
NM_000392.5(ABCC2):c.4317A>G (p.Ile1439Met) rs924936790
NM_000392.5(ABCC2):c.4350T>C (p.Ala1450=) rs1564703757
NM_000392.5(ABCC2):c.4439A>G (p.Gln1480Arg) rs1564703854
NM_000392.5(ABCC2):c.4449C>T (p.Phe1483=) rs756299268
NM_000392.5(ABCC2):c.4465_4473delinsGGCCCACAG (p.Ile1489_Ile1491delinsGlyProGln)
NM_000392.5(ABCC2):c.4466T>C (p.Ile1489Thr)
NM_000392.5(ABCC2):c.4494C>G (p.Ile1498Met) rs539252097
NM_000392.5(ABCC2):c.4532dup (p.Ile1512fs)
NM_000392.5(ABCC2):c.4538T>C (p.Ile1513Thr) rs1564704176
NM_000392.5(ABCC2):c.4555G>A (p.Glu1519Lys) rs1564704207
NM_000392.5(ABCC2):c.4561del (p.Leu1521fs) rs1554854998
NM_000392.5(ABCC2):c.4566A>C (p.Leu1522=) rs773138110
NM_000392.5(ABCC2):c.4580C>T (p.Pro1527Leu) rs776473749
NM_000392.5(ABCC2):c.4581C>T (p.Pro1527=) rs1564704231
NM_000392.5(ABCC2):c.524A>C (p.Gln175Pro)
NM_000392.5(ABCC2):c.601C>T (p.Leu201=) rs749655460
NM_000392.5(ABCC2):c.636C>A (p.Ile212=) rs1564673185
NM_000392.5(ABCC2):c.655C>G (p.Arg219Gly)
NM_000392.5(ABCC2):c.670G>A (p.Glu224Lys)
NM_000392.5(ABCC2):c.734A>G (p.His245Arg)
NM_000392.5(ABCC2):c.736A>T (p.Met246Leu) rs17222744

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.