ClinVar Miner

List of variants in gene GFM1 reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 47
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HGVS dbSNP gnomAD frequency
NM_024996.7(GFM1):c.840+108C>G rs55992564 0.02936
NM_024996.7(GFM1):c.1909+232A>C rs115801127 0.01598
NM_024996.7(GFM1):c.689+1184A>G rs142355183 0.01404
NM_024996.7(GFM1):c.1519-33A>T rs138856342 0.00601
NM_024996.7(GFM1):c.368-177G>A rs143692807 0.00564
NM_024996.7(GFM1):c.840+317T>C rs186196590 0.00564
NM_024996.7(GFM1):c.1222-321A>G rs184609675 0.00563
NM_024996.7(GFM1):c.1765-94C>T rs143940766 0.00393
NM_024996.7(GFM1):c.1221+222T>C rs145106063 0.00389
NM_024996.7(GFM1):c.1381-39C>T rs116646562 0.00356
NM_024996.7(GFM1):c.1221+203G>A rs116781201 0.00319
NM_024996.7(GFM1):c.1764+11A>T rs199739357 0.00265
NM_024996.7(GFM1):c.1909+41A>G rs114335950 0.00263
NM_024996.7(GFM1):c.2190C>T (p.Asp730=) rs149049400 0.00196
NM_024996.7(GFM1):c.368-34T>A rs527243547 0.00178
NM_024996.7(GFM1):c.788A>G (p.Gln263Arg) rs115984741 0.00158
NM_024996.7(GFM1):c.220G>T (p.Ala74Ser) rs140377587 0.00155
NM_024996.7(GFM1):c.235-85G>C rs181367389 0.00073
NM_024996.7(GFM1):c.1324-15T>A rs375168014 0.00057
NM_024996.7(GFM1):c.1032C>T (p.Asn344=) rs373952002 0.00036
NM_024996.7(GFM1):c.1494A>G (p.Glu498=) rs149454742 0.00029
NM_024996.7(GFM1):c.690-40G>A rs180934936 0.00024
NM_024996.7(GFM1):c.*9A>G rs372245257 0.00018
NM_024996.7(GFM1):c.597G>A (p.Ala199=) rs148209578 0.00011
NM_024996.7(GFM1):c.2059C>T (p.Leu687=) rs771619705 0.00007
NM_024996.7(GFM1):c.1377C>T (p.Asn459=) rs373098153 0.00004
NM_024996.7(GFM1):c.234+17G>A rs532180547 0.00004
NM_024996.7(GFM1):c.1626A>G (p.Gln542=) rs139042191 0.00002
NM_024996.7(GFM1):c.2071-20T>C rs531105833 0.00001
NM_024996.7(GFM1):c.*116C>T rs115593809
NM_024996.7(GFM1):c.-25C>T rs1057520288
NM_024996.7(GFM1):c.1065C>T (p.Gly355=) rs1722593482
NM_024996.7(GFM1):c.1083+3A>G rs187690169
NM_024996.7(GFM1):c.1084-299A>T rs115123609
NM_024996.7(GFM1):c.1221+323T>C rs76266615
NM_024996.7(GFM1):c.1519-211T>G rs2115940
NM_024996.7(GFM1):c.1909+131C>T rs114879672
NM_024996.7(GFM1):c.1909+13C>G rs141146379
NM_024996.7(GFM1):c.1909+13C>T rs141146379
NM_024996.7(GFM1):c.1910-8del rs34920045
NM_024996.7(GFM1):c.193C>A (p.Arg65=) rs62286651
NM_024996.7(GFM1):c.2125-11del rs747030381
NM_024996.7(GFM1):c.2125-11dup rs747030381
NM_024996.7(GFM1):c.2125-32_2125-30del rs552631941
NM_024996.7(GFM1):c.81+283dup rs11405116
NM_024996.7(GFM1):c.82-118A>G rs140204632
NM_024996.7(GFM1):c.82-198G>A rs7618421

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