ClinVar Miner

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

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Gene type:
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Total variants: 122
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HGVS dbSNP gnomAD frequency
NM_001364905.1(LRBA):c.5030A>G (p.Asn1677Ser) rs17027133 0.00349
NM_001364905.1(LRBA):c.1399A>G (p.Met467Val) rs116355217 0.00225
NM_001364905.1(LRBA):c.2444A>G (p.Asn815Ser) rs140666848 0.00218
NM_001364905.1(LRBA):c.2637G>A (p.Lys879=) rs138956153 0.00170
NM_001364905.1(LRBA):c.8551C>T (p.Arg2851Cys) rs145709687 0.00152
NM_001364905.1(LRBA):c.2340A>G (p.Thr780=) rs79392371 0.00127
NM_001364905.1(LRBA):c.6887C>A (p.Thr2296Asn) rs151286835 0.00113
NM_001364905.1(LRBA):c.1713C>T (p.His571=) rs145812385 0.00101
NM_001364905.1(LRBA):c.6662T>C (p.Ile2221Thr) rs116526975 0.00083
NM_001364905.1(LRBA):c.2209G>A (p.Val737Ile) rs151213445 0.00078
NM_001364905.1(LRBA):c.787C>G (p.Leu263Val) rs143625481 0.00076
NM_001364905.1(LRBA):c.6036C>T (p.Ala2012=) rs145411537 0.00068
NM_001364905.1(LRBA):c.8024C>T (p.Thr2675Ile) rs202244838 0.00067
NM_001364905.1(LRBA):c.8440C>T (p.Arg2814Trp) rs143351602 0.00066
NM_001364905.1(LRBA):c.3743A>G (p.Asn1248Ser) rs140860135 0.00056
NM_001364905.1(LRBA):c.2112G>A (p.Met704Ile) rs114786941 0.00041
NM_001364905.1(LRBA):c.1771T>C (p.Tyr591His) rs138890467 0.00038
NM_001364905.1(LRBA):c.3407C>T (p.Pro1136Leu) rs113022115 0.00033
NM_001364905.1(LRBA):c.4930C>G (p.Leu1644Val) rs149324157 0.00031
NM_001364905.1(LRBA):c.3499A>G (p.Thr1167Ala) rs146297781 0.00026
NM_001364905.1(LRBA):c.3262G>C (p.Glu1088Gln) rs142075710 0.00023
NM_001364905.1(LRBA):c.3914G>A (p.Arg1305His) rs144754728 0.00019
NM_001364905.1(LRBA):c.1161+4G>T rs374666604 0.00013
NM_001364905.1(LRBA):c.6848A>T (p.Asp2283Val) rs147096866 0.00012
NM_001364905.1(LRBA):c.2050C>T (p.Leu684=) rs149148368 0.00010
NM_001364905.1(LRBA):c.5876A>G (p.Asn1959Ser) rs369187914 0.00010
NM_001364905.1(LRBA):c.6827G>A (p.Arg2276His) rs200802435 0.00010
NM_001364905.1(LRBA):c.6921A>G (p.Ile2307Met) rs201643144 0.00009
NM_001364905.1(LRBA):c.7194+4A>G rs374748594 0.00009
NM_001364905.1(LRBA):c.7879T>C (p.Trp2627Arg) rs200295901 0.00009
NM_001364905.1(LRBA):c.8461G>A (p.Asp2821Asn) rs191145485 0.00009
NM_001364905.1(LRBA):c.1372G>A (p.Val458Ile) rs765483951 0.00008
NM_001364905.1(LRBA):c.4338A>G (p.Leu1446=) rs201059532 0.00008
NM_001364905.1(LRBA):c.5831A>G (p.Tyr1944Cys) rs150829802 0.00008
NM_001364905.1(LRBA):c.1931C>T (p.Pro644Leu) rs371718439 0.00007
NM_001364905.1(LRBA):c.2662G>A (p.Glu888Lys) rs200640538 0.00006
NM_001364905.1(LRBA):c.4793C>T (p.Ser1598Leu) rs370438098 0.00006
NM_001364905.1(LRBA):c.7888G>A (p.Val2630Ile) rs564067785 0.00005
NM_001364905.1(LRBA):c.3394A>T (p.Asn1132Tyr) rs769386027 0.00004
NM_001364905.1(LRBA):c.3942G>A (p.Met1314Ile) rs761765555 0.00004
NM_001364905.1(LRBA):c.5004G>A (p.Pro1668=) rs775567440 0.00004
NM_001364905.1(LRBA):c.5906G>C (p.Gly1969Ala) rs745608560 0.00004
NM_001364905.1(LRBA):c.7795A>G (p.Ile2599Val) rs1288341022 0.00004
NM_001364905.1(LRBA):c.7859T>G (p.Ile2620Ser) rs777084152 0.00004
NM_001364905.1(LRBA):c.1259C>T (p.Thr420Met) rs1042175189 0.00003
NM_001364905.1(LRBA):c.1316A>G (p.Asn439Ser) rs572309256 0.00003
NM_001364905.1(LRBA):c.3207C>A (p.Gly1069=) rs762031957 0.00003
NM_001364905.1(LRBA):c.7571C>G (p.Ala2524Gly) rs145552628 0.00003
NM_001364905.1(LRBA):c.1008T>C (p.Thr336=) rs747214029 0.00002
NM_001364905.1(LRBA):c.3202A>G (p.Thr1068Ala) rs375113636 0.00002
NM_001364905.1(LRBA):c.3244A>G (p.Ile1082Val) rs553088346 0.00002
NM_001364905.1(LRBA):c.5434C>T (p.Arg1812Cys) rs368625168 0.00002
NM_001364905.1(LRBA):c.782A>G (p.Lys261Arg) rs375175981 0.00002
NM_001364905.1(LRBA):c.1180G>C (p.Ala394Pro) rs753848083 0.00001
NM_001364905.1(LRBA):c.1433C>T (p.Pro478Leu) rs896257229 0.00001
NM_001364905.1(LRBA):c.1573T>G (p.Phe525Val) rs768302925 0.00001
NM_001364905.1(LRBA):c.1774A>G (p.Thr592Ala) rs373175911 0.00001
NM_001364905.1(LRBA):c.240G>A (p.Leu80=) rs765297527 0.00001
NM_001364905.1(LRBA):c.2516G>A (p.Arg839His) rs1022511990 0.00001
NM_001364905.1(LRBA):c.281G>T (p.Cys94Phe) rs771839194 0.00001
NM_001364905.1(LRBA):c.3742A>G (p.Asn1248Asp) rs1030048061 0.00001
NM_001364905.1(LRBA):c.4300A>T (p.Met1434Leu) rs1487349620 0.00001
NM_001364905.1(LRBA):c.4763C>T (p.Thr1588Met) rs150879069 0.00001
NM_001364905.1(LRBA):c.4919T>C (p.Val1640Ala) rs773862243 0.00001
NM_001364905.1(LRBA):c.4975G>A (p.Gly1659Arg) rs1746594596 0.00001
NM_001364905.1(LRBA):c.5084T>C (p.Val1695Ala) rs200935054 0.00001
NM_001364905.1(LRBA):c.6037G>A (p.Val2013Met) rs747204894 0.00001
NM_001364905.1(LRBA):c.6049A>C (p.Thr2017Pro) rs371434395 0.00001
NM_001364905.1(LRBA):c.6074G>A (p.Gly2025Glu) rs778545671 0.00001
NM_001364905.1(LRBA):c.6553C>T (p.Arg2185Cys) rs764408115 0.00001
NM_001364905.1(LRBA):c.6664G>A (p.Ala2222Thr) rs754600521 0.00001
NM_001364905.1(LRBA):c.7010G>A (p.Arg2337Gln) rs1198087317 0.00001
NM_001364905.1(LRBA):c.7339A>G (p.Ile2447Val) rs754778401 0.00001
NM_001364905.1(LRBA):c.7623C>T (p.Asn2541=) rs758608400 0.00001
NM_001364905.1(LRBA):c.7865T>C (p.Val2622Ala) rs541116943 0.00001
NM_001364905.1(LRBA):c.8064G>T (p.Glu2688Asp) rs984876178 0.00001
NM_001364905.1(LRBA):c.8426G>A (p.Cys2809Tyr) rs1470296037 0.00001
NM_001364905.1(LRBA):c.8531G>A (p.Trp2844Ter) rs1323561325 0.00001
GRCh37/hg19 4q31.3(chr4:151284899-151403757)x3
GRCh37/hg19 4q31.3(chr4:151803708-151953453)x1
NM_001364905.1(LRBA):c.1015-9C>A rs765923836
NM_001364905.1(LRBA):c.114G>T (p.Gly38=) rs72721739
NM_001364905.1(LRBA):c.1802C>T (p.Thr601Ile) rs369623654
NM_001364905.1(LRBA):c.1924+4_1924+7del rs1355259232
NM_001364905.1(LRBA):c.2338A>G (p.Thr780Ala) rs1273184429
NM_001364905.1(LRBA):c.2439A>G (p.Ile813Met) rs2127000700
NM_001364905.1(LRBA):c.3056T>A (p.Met1019Lys) rs2126923027
NM_001364905.1(LRBA):c.3196A>G (p.Ile1066Val)
NM_001364905.1(LRBA):c.3307G>C (p.Glu1103Gln) rs794727384
NM_001364905.1(LRBA):c.3373C>G (p.Leu1125Val) rs138238756
NM_001364905.1(LRBA):c.3583A>G (p.Thr1195Ala)
NM_001364905.1(LRBA):c.3789C>T (p.Asn1263=) rs150689413
NM_001364905.1(LRBA):c.3829T>C (p.Ser1277Pro) rs765914410
NM_001364905.1(LRBA):c.3856G>A (p.Gly1286Arg) rs2126915521
NM_001364905.1(LRBA):c.4080C>T (p.Leu1360=)
NM_001364905.1(LRBA):c.4112C>T (p.Ala1371Val) rs1578989457
NM_001364905.1(LRBA):c.4228C>G (p.Leu1410Val) rs1578987261
NM_001364905.1(LRBA):c.4339+4A>C rs2126904793
NM_001364905.1(LRBA):c.4340-5T>C rs2126887700
NM_001364905.1(LRBA):c.4723C>T (p.Leu1575Phe) rs1182264315
NM_001364905.1(LRBA):c.4907C>G (p.Ala1636Gly) rs1315950546
NM_001364905.1(LRBA):c.5069C>T (p.Ala1690Val)
NM_001364905.1(LRBA):c.5456C>T (p.Ala1819Val)
NM_001364905.1(LRBA):c.549+6A>C rs199594598
NM_001364905.1(LRBA):c.5522T>C (p.Leu1841Pro) rs752995422
NM_001364905.1(LRBA):c.5786G>A (p.Arg1929Gln) rs747575946
NM_001364905.1(LRBA):c.6046+1900T>G rs886042789
NM_001364905.1(LRBA):c.6274G>A (p.Glu2092Lys) rs769501419
NM_001364905.1(LRBA):c.6322G>A (p.Asp2108Asn) rs142598024
NM_001364905.1(LRBA):c.6512G>T (p.Arg2171Leu) rs572317255
NM_001364905.1(LRBA):c.6552-13C>G rs140629626
NM_001364905.1(LRBA):c.6667+5C>G rs751485504
NM_001364905.1(LRBA):c.6735A>T (p.Glu2245Asp)
NM_001364905.1(LRBA):c.6766A>G (p.Arg2256Gly) rs1561218846
NM_001364905.1(LRBA):c.7019A>G (p.Gln2340Arg) rs2151993396
NM_001364905.1(LRBA):c.7195-12_7195-9dup rs1561051659
NM_001364905.1(LRBA):c.7283G>C (p.Arg2428Pro) rs139563734
NM_001364905.1(LRBA):c.7316A>G (p.Glu2439Gly) rs752621759
NM_001364905.1(LRBA):c.7619A>G (p.His2540Arg) rs2126925023
NM_001364905.1(LRBA):c.8350C>T (p.Leu2784Phe) rs867668931
NM_001364905.1(LRBA):c.840G>C (p.Lys280Asn) rs1344342751
NM_001364905.1(LRBA):c.8450C>T (p.Ala2817Val) rs142943481

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