ClinVar Miner

List of variants reported as benign for Multiple endocrine neoplasia

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ClinVar version:
Total variants: 52
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HGVS dbSNP gnomAD frequency
NM_020975.6(RET):c.*1506G>A rs2742241 0.83094
NM_020630.5(RET):c.-200A>G rs10900296 0.77447
NM_020975.6(RET):c.1296A>G (p.Ala432=) rs1800860 0.74268
NM_020975.6(RET):c.*1116T>C rs2435355 0.22170
NM_020975.6(RET):c.2712C>G (p.Ser904=) rs1800863 0.17043
NM_020975.6(RET):c.*388G>A rs3026782 0.17032
NM_020975.6(RET):c.*95C>T rs17028 0.16697
NM_020975.6(RET):c.2508C>T (p.Ser836=) rs1800862 0.03791
NM_020975.6(RET):c.*1591G>A rs76759170 0.03751
NM_020975.6(RET):c.2944C>T (p.Arg982Cys) rs17158558 0.01567
NM_001370259.2(MEN1):c.512G>A (p.Arg171Gln) rs607969 0.01309
NM_020975.6(RET):c.375C>A (p.Val125=) rs1800859 0.00877
NM_020975.6(RET):c.*330A>G rs141460872 0.00640
NM_020975.6(RET):c.*1870C>T rs146771196 0.00539
NM_020975.6(RET):c.166C>A (p.Leu56Met) rs145633958 0.00310
NM_020975.6(RET):c.*1583G>A rs192065891 0.00300
NM_020975.6(RET):c.*1599G>A rs145954635 0.00265
NM_020975.6(RET):c.*1558A>C rs142572876 0.00260
NM_020975.6(RET):c.1336G>C (p.Gly446Arg) rs115423919 0.00238
NM_020975.6(RET):c.*1812C>A rs183817000 0.00220
NM_020975.6(RET):c.654G>A (p.Pro218=) rs137928436 0.00138
NM_020975.6(RET):c.*1130A>G rs572936041 0.00112
NM_020975.6(RET):c.1119G>A (p.Ala373=) rs113931414 0.00079
NM_020975.6(RET):c.833C>A (p.Thr278Asn) rs35118262 0.00056
NM_020975.6(RET):c.225G>A (p.Thr75=) rs151267865 0.00052
NM_020975.6(RET):c.*29C>A rs199639914 0.00050
NM_020975.6(RET):c.3112A>G (p.Thr1038Ala) rs201740483 0.00047
NM_020975.6(RET):c.*576G>A rs185408658 0.00044
NM_020975.6(RET):c.*1644G>C rs117119161 0.00043
NM_020975.6(RET):c.*1348G>A rs149252070 0.00039
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.341G>A (p.Arg114His) rs76397662 0.00029
NM_020975.6(RET):c.2052G>A (p.Pro684=) rs145122337 0.00019
NM_020975.6(RET):c.1699G>A (p.Asp567Asn) rs147219360 0.00014
NM_020975.6(RET):c.597C>T (p.Asn199=) rs55810667 0.00012
NM_020975.6(RET):c.1353G>T (p.Thr451=) rs201568301 0.00010
NM_020975.6(RET):c.3243T>C (p.Asp1081=) rs144192900 0.00010
NM_020975.6(RET):c.1879+13C>T rs375573788 0.00008
NM_020975.6(RET):c.*1326T>C rs141016377 0.00007
NM_020975.6(RET):c.2418C>T (p.Tyr806=) rs553418132 0.00005
NM_020975.6(RET):c.3188-9C>T rs551159582 0.00005
NM_020975.6(RET):c.2976G>A (p.Pro992=) rs528823385 0.00004
NM_020975.6(RET):c.220G>A (p.Gly74Ser) rs764938319 0.00002
NM_020975.6(RET):c.235C>T (p.Arg79Trp) rs537523906 0.00001
NM_020975.6(RET):c.*1046G>C rs143948954
NM_020975.6(RET):c.*492G>C rs568766449
NM_020975.6(RET):c.-160G>T rs567112195
NM_020975.6(RET):c.1523-7C>T rs567967877
NM_020975.6(RET):c.2393-14C>T rs144269978
NM_020975.6(RET):c.487C>A (p.Arg163=) rs371153966

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