ClinVar Miner

List of variants in gene RET reported as likely benign for adrenal gland disease

Included ClinVar conditions (124):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 73
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HGVS dbSNP
NM_020630.5(RET):c.2372A>T (p.Tyr791Phe) rs77724903
NM_020975.5(RET):c.2137-16del rs1409965349
NM_020975.6(RET):c.*1116T>C rs2435355
NM_020975.6(RET):c.*1558A>C rs142572876
NM_020975.6(RET):c.*1583G>A rs192065891
NM_020975.6(RET):c.*1591G>A rs76759170
NM_020975.6(RET):c.*1599G>A rs145954635
NM_020975.6(RET):c.*1742G>A rs143369221
NM_020975.6(RET):c.*1870C>T rs146771196
NM_020975.6(RET):c.*1969T>C rs3026785
NM_020975.6(RET):c.*330A>G rs141460872
NM_020975.6(RET):c.*388G>A rs3026782
NM_020975.6(RET):c.*499dup rs201945709
NM_020975.6(RET):c.*576G>A rs185408658
NM_020975.6(RET):c.*95C>T rs17028
NM_020975.6(RET):c.1017G>A (p.Ser339=) rs369810881
NM_020975.6(RET):c.1095G>A (p.Ser365=) rs201992974
NM_020975.6(RET):c.1118C>T (p.Ala373Val) rs546866208
NM_020975.6(RET):c.1182C>T (p.Asn394=) rs376465385
NM_020975.6(RET):c.1188G>A (p.Ser396=) rs758510657
NM_020975.6(RET):c.1197G>A (p.Pro399=) rs148371113
NM_020975.6(RET):c.1264-4C>T rs587780806
NM_020975.6(RET):c.1264-5C>T rs9282835
NM_020975.6(RET):c.1336G>C (p.Gly446Arg) rs115423919
NM_020975.6(RET):c.1437C>T (p.Ala479=) rs576806356
NM_020975.6(RET):c.1522+35C>T rs377130948
NM_020975.6(RET):c.1523-7C>T rs567967877
NM_020975.6(RET):c.1530C>T (p.Ala510=) rs553492964
NM_020975.6(RET):c.1648+24G>A rs1057517640
NM_020975.6(RET):c.1649-4G>A rs369769303
NM_020975.6(RET):c.1760-12G>A rs377767392
NM_020975.6(RET):c.1879+13C>T rs375573788
NM_020975.6(RET):c.1879+14G>A rs532810255
NM_020975.6(RET):c.1879+17C>T rs369920430
NM_020975.6(RET):c.1893C>T (p.Asp631=) rs55846256
NM_020975.6(RET):c.1942G>A (p.Val648Ile) rs77711105
NM_020975.6(RET):c.1946C>T (p.Ser649Leu) rs148935214
NM_020975.6(RET):c.200G>A (p.Arg67His) rs192489011
NM_020975.6(RET):c.2037C>T (p.Pro679=) rs55862116
NM_020975.6(RET):c.2070C>T (p.Ser690=) rs201550433
NM_020975.6(RET):c.2071G>A (p.Gly691Ser) rs1799939
NM_020975.6(RET):c.2088G>A (p.Ser696=) rs150329150
NM_020975.6(RET):c.2136+15G>A rs751183869
NM_020975.6(RET):c.2226G>A (p.Thr742=) rs762876946
NM_020975.6(RET):c.225G>A (p.Thr75=) rs151267865
NM_020975.6(RET):c.2284+54C>A rs566375223
NM_020975.6(RET):c.2285-4T>G rs376601566
NM_020975.6(RET):c.2298G>A (p.Pro766=) rs140658743
NM_020975.6(RET):c.2393-9C>T rs567543719
NM_020975.6(RET):c.2409C>T (p.Ile803=) rs535051804
NM_020975.6(RET):c.2508C>T (p.Ser836=) rs1800862
NM_020975.6(RET):c.2523G>A (p.Pro841=) rs56195026
NM_020975.6(RET):c.262A>G (p.Ile88Val) rs141679950
NM_020975.6(RET):c.2712C>G (p.Ser904=) rs1800863
NM_020975.6(RET):c.2715C>T (p.Tyr905=) rs755023496
NM_020975.6(RET):c.2802-4G>T rs878855061
NM_020975.6(RET):c.2944C>T (p.Arg982Cys) rs17158558
NM_020975.6(RET):c.2976G>A (p.Pro992=) rs528823385
NM_020975.6(RET):c.2988G>A (p.Pro996=) rs145798106
NM_020975.6(RET):c.3040-11C>G rs1057517646
NM_020975.6(RET):c.3057G>A (p.Ala1019=) rs369579749
NM_020975.6(RET):c.3112A>G (p.Thr1038Ala) rs201740483
NM_020975.6(RET):c.3243T>C (p.Asp1081=) rs144192900
NM_020975.6(RET):c.337+11C>T rs754967305
NM_020975.6(RET):c.337+12G>A rs200468424
NM_020975.6(RET):c.337+29G>A rs578158807
NM_020975.6(RET):c.337+34C>T rs368088467
NM_020975.6(RET):c.337+9G>A rs2435351
NM_020975.6(RET):c.375C>A (p.Val125=) rs1800859
NM_020975.6(RET):c.654G>A (p.Pro218=) rs137928436
NM_020975.6(RET):c.693C>T (p.Arg231=) rs576806329
NM_020975.6(RET):c.785T>C (p.Val262Ala) rs139790943
NM_020975.6(RET):c.874G>A (p.Val292Met) rs34682185

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