ClinVar Miner

List of variants in gene RET reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 86
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HGVS dbSNP gnomAD frequency
NM_020975.6(RET):c.*1591G>A rs76759170 0.03751
NM_020975.6(RET):c.2392+159G>A rs3026767 0.02002
NM_020975.6(RET):c.2801+225C>T rs7923702 0.01430
NM_020975.6(RET):c.73+104C>T rs111514357 0.01331
NM_020975.6(RET):c.625+139C>T rs115766280 0.01278
NM_020975.6(RET):c.626-189_626-180del rs546164092 0.01153
NM_020975.6(RET):c.867+166G>A rs112933094 0.01027
NM_020975.6(RET):c.1064-114G>A rs3026742 0.01008
NM_020975.6(RET):c.337+196G>A rs115330432 0.00704
NM_020975.6(RET):c.868-63G>C rs146623661 0.00645
NM_020975.6(RET):c.73+188G>A rs866591037 0.00618
NM_020975.6(RET):c.338-201C>G rs112976896 0.00592
NM_020975.6(RET):c.868-86A>G rs112753528 0.00589
NM_020975.6(RET):c.337+247C>T rs112451273 0.00583
NM_020975.6(RET):c.1264-196G>A rs77890871 0.00568
NM_020975.6(RET):c.2608-117G>T rs150916310 0.00541
NM_020975.6(RET):c.2607+136A>G rs571991475 0.00529
NM_020975.6(RET):c.626-151G>A rs188616637 0.00444
NM_020975.6(RET):c.867+171A>T rs3026739 0.00436
NM_020975.6(RET):c.2284+46G>C rs147601354 0.00420
NM_020975.6(RET):c.2939+258G>A rs116380716 0.00365
NM_020975.6(RET):c.166C>A (p.Leu56Met) rs145633958 0.00310
NM_020975.6(RET):c.1063+145A>G rs182113946 0.00260
NM_020975.6(RET):c.1336G>C (p.Gly446Arg) rs115423919 0.00238
NM_020975.6(RET):c.337+12G>A rs200468424 0.00198
NM_020975.6(RET):c.468C>T (p.Ala156=) rs141290380 0.00173
NM_020975.6(RET):c.654G>A (p.Pro218=) rs137928436 0.00138
NM_020975.6(RET):c.1197G>A (p.Pro399=) rs148371113 0.00108
NM_020975.6(RET):c.1119G>A (p.Ala373=) rs113931414 0.00079
NM_020975.6(RET):c.1124T>A (p.Leu375Gln) rs142338976 0.00073
NM_020975.6(RET):c.262A>G (p.Ile88Val) rs141679950 0.00056
NM_020975.6(RET):c.225G>A (p.Thr75=) rs151267865 0.00052
NM_020975.6(RET):c.405C>T (p.Gly135=) rs142345108 0.00051
NM_020975.6(RET):c.3112A>G (p.Thr1038Ala) rs201740483 0.00047
NM_020975.6(RET):c.1354C>A (p.Leu452Ile) rs151148041 0.00043
NM_020975.6(RET):c.1946C>T (p.Ser649Leu) rs148935214 0.00039
NM_020975.6(RET):c.2037C>T (p.Pro679=) rs55862116 0.00039
NM_020975.6(RET):c.1158G>A (p.Ala386=) rs373540097 0.00034
NM_020975.6(RET):c.2673G>A (p.Ser891=) rs201620214 0.00027
NM_020975.6(RET):c.2088G>A (p.Ser696=) rs150329150 0.00024
NM_020975.6(RET):c.785T>C (p.Val262Ala) rs139790943 0.00024
NM_020975.6(RET):c.3040-20C>T rs372172456 0.00020
NM_020975.6(RET):c.1529C>T (p.Ala510Val) rs201745826 0.00019
NM_020975.6(RET):c.2052G>A (p.Pro684=) rs145122337 0.00019
NM_020975.6(RET):c.1063+9G>A rs765463636 0.00014
NM_020975.6(RET):c.1699G>A (p.Asp567Asn) rs147219360 0.00014
NM_020975.6(RET):c.1701C>T (p.Asp567=) rs201209972 0.00014
NM_020975.6(RET):c.2988G>A (p.Pro996=) rs145798106 0.00014
NM_020975.6(RET):c.1893C>T (p.Asp631=) rs55846256 0.00013
NM_020975.6(RET):c.597C>T (p.Asn199=) rs55810667 0.00012
NM_020975.6(RET):c.957C>A (p.Leu319=) rs149926238 0.00011
NM_020975.6(RET):c.1596C>T (p.Gly532=) rs144460361 0.00008
NM_020975.6(RET):c.1942G>A (p.Val648Ile) rs77711105 0.00007
NM_020975.6(RET):c.204G>T (p.Leu68=) rs148874112 0.00007
NM_020975.6(RET):c.3336T>C (p.Phe1112=) rs146049841 0.00007
NM_020975.6(RET):c.81G>A (p.Leu27=) rs369519655 0.00007
NM_020975.6(RET):c.1118C>T (p.Ala373Val) rs546866208 0.00004
NM_020975.6(RET):c.1438G>A (p.Glu480Lys) rs537874538 0.00004
NM_020975.6(RET):c.2976G>A (p.Pro992=) rs528823385 0.00004
NM_020975.6(RET):c.2392+19T>C rs778745375 0.00003
NM_020975.6(RET):c.3138C>A (p.Ala1046=) rs201576838 0.00003
NM_020975.6(RET):c.144G>A (p.Thr48=) rs759872307 0.00002
NM_020975.6(RET):c.2358T>C (p.His786=) rs758715544 0.00002
NM_020975.6(RET):c.1221C>T (p.Thr407=) rs1222385123 0.00001
NM_020975.6(RET):c.1374C>T (p.Ala458=) rs190750926 0.00001
NM_020975.6(RET):c.1464C>T (p.Thr488=) rs921948385 0.00001
NM_020975.6(RET):c.1890C>T (p.Cys630=) rs781145070 0.00001
NM_020975.6(RET):c.2934G>A (p.Glu978=) rs767306671 0.00001
NM_020975.6(RET):c.2939+20G>A rs201756161 0.00001
NM_020975.6(RET):c.3057G>A (p.Ala1019=) rs369579749 0.00001
NM_020975.6(RET):c.1263+57del rs34903010
NM_020975.6(RET):c.1353G>A (p.Thr451=) rs201568301
NM_020975.6(RET):c.1523-12T>G rs1429462039
NM_020975.6(RET):c.1649-11G>T rs746325077
NM_020975.6(RET):c.2284+54C>A rs566375223
NM_020975.6(RET):c.2393-5C>T rs1554819512
NM_020975.6(RET):c.2523G>A (p.Pro841=) rs56195026
NM_020975.6(RET):c.2523G>T (p.Pro841=) rs56195026
NM_020975.6(RET):c.2801+243G>C rs3026774
NM_020975.6(RET):c.2939+110del rs201104591
NM_020975.6(RET):c.2939+286A>G rs76718568
NM_020975.6(RET):c.337+258G>T rs191765389
NM_020975.6(RET):c.338-174_338-162del rs148863289
NM_020975.6(RET):c.487C>A (p.Arg163=) rs371153966
NM_020975.6(RET):c.74-158G>T rs112834982
NM_020975.6(RET):c.74-58_74-57dup rs57003029

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