ClinVar Miner

List of variants in gene XYLT2 reported as uncertain significance for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 126
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_022167.4(XYLT2):c.1841C>T (p.Ala614Val) rs149423854 0.00084
NM_022167.4(XYLT2):c.290G>A (p.Arg97Gln) rs201002166 0.00050
NM_022167.4(XYLT2):c.698G>A (p.Arg233Gln) rs142606378 0.00041
NM_022167.4(XYLT2):c.1708G>A (p.Ala570Thr) rs199816555 0.00021
NM_022167.4(XYLT2):c.1600A>G (p.Lys534Glu) rs370444515 0.00017
NM_022167.4(XYLT2):c.1859C>T (p.Thr620Met) rs368387862 0.00014
NM_022167.4(XYLT2):c.1271G>A (p.Arg424His) rs141143630 0.00013
NM_022167.4(XYLT2):c.811G>A (p.Asp271Asn) rs138933160 0.00013
NM_022167.4(XYLT2):c.281A>C (p.Lys94Thr) rs558268220 0.00012
NM_022167.4(XYLT2):c.371G>C (p.Ser124Thr) rs368979862 0.00012
NM_022167.4(XYLT2):c.643G>A (p.Gly215Ser) rs148860176 0.00012
NM_022167.4(XYLT2):c.493G>A (p.Val165Met) rs201070818 0.00009
NM_022167.4(XYLT2):c.1820C>T (p.Thr607Met) rs138319215 0.00007
NM_022167.4(XYLT2):c.439G>A (p.Val147Met) rs779253497 0.00007
NM_022167.4(XYLT2):c.1474C>T (p.Arg492Trp) rs375521710 0.00006
NM_022167.4(XYLT2):c.289C>T (p.Arg97Trp) rs199498175 0.00006
NM_022167.4(XYLT2):c.824G>A (p.Arg275Gln) rs199983537 0.00006
NM_022167.4(XYLT2):c.1942-8C>G rs1014512062 0.00005
NM_022167.4(XYLT2):c.2225G>A (p.Arg742His) rs369581548 0.00005
NM_022167.4(XYLT2):c.2312A>G (p.Asn771Ser) rs199705453 0.00005
NM_022167.4(XYLT2):c.2584G>A (p.Gly862Arg) rs368411795 0.00005
NM_022167.4(XYLT2):c.311G>A (p.Arg104Lys) rs759939858 0.00005
NM_022167.4(XYLT2):c.527C>T (p.Ala176Val) rs143167798 0.00005
NM_022167.4(XYLT2):c.763G>A (p.Val255Ile) rs373326489 0.00005
NM_022167.4(XYLT2):c.1089G>A (p.Arg363=) rs200160055 0.00004
NM_022167.4(XYLT2):c.1726A>G (p.Met576Val) rs200430765 0.00004
NM_022167.4(XYLT2):c.487G>A (p.Glu163Lys) rs201066232 0.00004
NM_022167.4(XYLT2):c.1075C>T (p.Arg359Trp) rs752699422 0.00003
NM_022167.4(XYLT2):c.1354G>A (p.Val452Met) rs139052712 0.00003
NM_022167.4(XYLT2):c.1450G>A (p.Asp484Asn) rs563509039 0.00003
NM_022167.4(XYLT2):c.1826C>T (p.Ala609Val) rs752138305 0.00003
NM_022167.4(XYLT2):c.2080A>G (p.Thr694Ala) rs145098209 0.00003
NM_022167.4(XYLT2):c.2420C>T (p.Ala807Val) rs565634363 0.00003
NM_022167.4(XYLT2):c.251G>A (p.Arg84His) rs766625947 0.00003
NM_022167.4(XYLT2):c.320G>A (p.Arg107Gln) rs761254841 0.00003
NM_022167.4(XYLT2):c.424G>A (p.Gly142Arg) rs371855496 0.00003
NM_022167.4(XYLT2):c.859G>A (p.Val287Met) rs200767788 0.00003
NM_022167.4(XYLT2):c.869C>T (p.Thr290Met) rs745745346 0.00003
NM_022167.4(XYLT2):c.929G>C (p.Ser310Thr) rs1282082560 0.00003
NM_022167.4(XYLT2):c.1132G>A (p.Asp378Asn) rs142963935 0.00002
NM_022167.4(XYLT2):c.1924C>T (p.Arg642Trp) rs201387055 0.00002
NM_022167.4(XYLT2):c.2345G>C (p.Ser782Thr) rs201353829 0.00002
NM_022167.4(XYLT2):c.29T>A (p.Leu10Gln) rs1336159526 0.00002
NM_022167.4(XYLT2):c.344C>T (p.Pro115Leu) rs748114111 0.00002
NM_022167.4(XYLT2):c.611G>A (p.Arg204Gln) rs370835556 0.00002
NM_022167.4(XYLT2):c.742C>G (p.Leu248Val) rs760893167 0.00002
NM_022167.4(XYLT2):c.1007+6G>A rs777998528 0.00001
NM_022167.4(XYLT2):c.1114C>T (p.Arg372Trp) rs1400942917 0.00001
NM_022167.4(XYLT2):c.1147C>T (p.Arg383Cys) rs1483985025 0.00001
NM_022167.4(XYLT2):c.1178T>C (p.Ile393Thr) rs888594669 0.00001
NM_022167.4(XYLT2):c.1319C>T (p.Thr440Met) rs758112079 0.00001
NM_022167.4(XYLT2):c.1337T>C (p.Leu446Pro) rs754679651 0.00001
NM_022167.4(XYLT2):c.1347G>C (p.Glu449Asp) rs748043559 0.00001
NM_022167.4(XYLT2):c.144G>T (p.Arg48Ser) rs777339294 0.00001
NM_022167.4(XYLT2):c.1482+3G>A rs1598351654 0.00001
NM_022167.4(XYLT2):c.1499C>T (p.Thr500Ile) rs772058919 0.00001
NM_022167.4(XYLT2):c.1573A>T (p.Ser525Cys) rs1447889654 0.00001
NM_022167.4(XYLT2):c.1585G>A (p.Gly529Ser) rs373514905 0.00001
NM_022167.4(XYLT2):c.1627G>A (p.Ala543Thr) rs751743242 0.00001
NM_022167.4(XYLT2):c.1628C>T (p.Ala543Val) rs755122467 0.00001
NM_022167.4(XYLT2):c.1738C>T (p.Leu580Phe) rs779329565 0.00001
NM_022167.4(XYLT2):c.1766C>T (p.Pro589Leu) rs1162733060 0.00001
NM_022167.4(XYLT2):c.2038C>T (p.Arg680Trp) rs779155720 0.00001
NM_022167.4(XYLT2):c.2039G>A (p.Arg680Gln) rs139687876 0.00001
NM_022167.4(XYLT2):c.2089G>A (p.Val697Met) rs1210911054 0.00001
NM_022167.4(XYLT2):c.2155A>G (p.Ser719Gly) rs1912648730 0.00001
NM_022167.4(XYLT2):c.2255G>A (p.Arg752His) rs775076771 0.00001
NM_022167.4(XYLT2):c.2369C>T (p.Pro790Leu) rs200597907 0.00001
NM_022167.4(XYLT2):c.2546C>G (p.Pro849Arg) rs770789907 0.00001
NM_022167.4(XYLT2):c.2588G>A (p.Arg863Gln) rs765678964 0.00001
NM_022167.4(XYLT2):c.32T>G (p.Val11Gly) rs1269448385 0.00001
NM_022167.4(XYLT2):c.5T>G (p.Val2Gly) rs1472707539 0.00001
NM_022167.4(XYLT2):c.604G>A (p.Val202Met) rs745496860 0.00001
NM_022167.4(XYLT2):c.617G>C (p.Cys206Ser) rs776590366 0.00001
NM_022167.4(XYLT2):c.637A>G (p.Ser213Gly) rs745332027 0.00001
NM_022167.4(XYLT2):c.692C>T (p.Pro231Leu) rs773062021 0.00001
NM_022167.4(XYLT2):c.728G>A (p.Arg243His) rs1315395627 0.00001
NM_022167.4(XYLT2):c.749G>A (p.Arg250His) rs1454779962 0.00001
NM_022167.4(XYLT2):c.761C>T (p.Ala254Val) rs779679769 0.00001
NM_022167.4(XYLT2):c.806G>C (p.Arg269Pro) rs775662377 0.00001
NM_022167.4(XYLT2):c.907C>T (p.Leu303Phe) rs1348568204 0.00001
NM_022167.4(XYLT2):c.926G>A (p.Arg309Gln) rs376174972 0.00001
NM_022167.4(XYLT2):c.934C>T (p.Arg312Trp) rs761643084 0.00001
NM_022167.4(XYLT2):c.1004C>T (p.Thr335Ile) rs1238032149
NM_022167.4(XYLT2):c.1216C>T (p.Arg406Cys) rs2543951751
NM_022167.4(XYLT2):c.1231_1232delinsGG (p.Tyr411Gly) rs2543951783
NM_022167.4(XYLT2):c.1247A>G (p.Asp416Gly) rs2543951840
NM_022167.4(XYLT2):c.1249G>C (p.Asp417His) rs2543951852
NM_022167.4(XYLT2):c.1336C>T (p.Leu446=)
NM_022167.4(XYLT2):c.1569_1570inv (p.Gly524Ser)
NM_022167.4(XYLT2):c.1582C>A (p.Pro528Thr)
NM_022167.4(XYLT2):c.1582C>T (p.Pro528Ser) rs147847688
NM_022167.4(XYLT2):c.1583C>A (p.Pro528His) rs369917912
NM_022167.4(XYLT2):c.1583C>T (p.Pro528Leu) rs369917912
NM_022167.4(XYLT2):c.1636G>T (p.Gly546Cys)
NM_022167.4(XYLT2):c.1735C>G (p.Pro579Ala) rs749710337
NM_022167.4(XYLT2):c.1753C>T (p.Pro585Ser) rs770825174
NM_022167.4(XYLT2):c.1773C>A (p.Ser591Arg) rs769862588
NM_022167.4(XYLT2):c.1792GAC[1] (p.Asp599del) rs1567807866
NM_022167.4(XYLT2):c.1853C>T (p.Ala618Val) rs2543956217
NM_022167.4(XYLT2):c.193G>A (p.Asp65Asn) rs1211266718
NM_022167.4(XYLT2):c.2010C>A (p.Asp670Glu)
NM_022167.4(XYLT2):c.2023G>T (p.Val675Leu) rs147831067
NM_022167.4(XYLT2):c.2107A>G (p.Ile703Val) rs369278935
NM_022167.4(XYLT2):c.2158C>T (p.Arg720Trp)
NM_022167.4(XYLT2):c.2176C>T (p.Pro726Ser) rs1598353144
NM_022167.4(XYLT2):c.217A>G (p.Ser73Gly) rs1912364733
NM_022167.4(XYLT2):c.2185G>C (p.Val729Leu) rs1163244585
NM_022167.4(XYLT2):c.2360T>G (p.Leu787Arg) rs2543963400
NM_022167.4(XYLT2):c.2402C>T (p.Thr801Ile) rs6504649
NM_022167.4(XYLT2):c.2535C>G (p.Ser845Arg)
NM_022167.4(XYLT2):c.2587C>T (p.Arg863Ter) rs762129763
NM_022167.4(XYLT2):c.2594G>A (p.Arg865Lys)
NM_022167.4(XYLT2):c.299C>G (p.Thr100Ser) rs773514375
NM_022167.4(XYLT2):c.350C>T (p.Ala117Val)
NM_022167.4(XYLT2):c.436A>T (p.Ser146Cys) rs2543946047
NM_022167.4(XYLT2):c.496G>A (p.Gly166Ser) rs764195134
NM_022167.4(XYLT2):c.509T>C (p.Leu170Pro) rs1555595456
NM_022167.4(XYLT2):c.544C>A (p.Gln182Lys) rs1053209381
NM_022167.4(XYLT2):c.655G>A (p.Asp219Asn)
NM_022167.4(XYLT2):c.671A>G (p.Gln224Arg)
NM_022167.4(XYLT2):c.793C>T (p.His265Tyr) rs1382213550
NM_022167.4(XYLT2):c.811G>C (p.Asp271His) rs138933160
NM_022167.4(XYLT2):c.823C>T (p.Arg275Trp) rs762208911
NM_022167.4(XYLT2):c.914_915delinsCA (p.Arg305Thr) rs2543949422
NM_022167.4(XYLT2):c.949G>A (p.Val317Met) rs1912457606

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.