ClinVar Miner

List of variants in gene GFM2 reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 42
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HGVS dbSNP gnomAD frequency
NM_032380.5(GFM2):c.2028+264A>G rs62366372 0.02764
NM_032380.5(GFM2):c.-24-179A>T rs147231258 0.01613
NM_032380.5(GFM2):c.1727-269C>G rs114172835 0.01586
NM_032380.5(GFM2):c.609-238C>A rs34833477 0.01538
NM_032380.5(GFM2):c.520-178G>A rs114282130 0.01435
NM_032380.5(GFM2):c.849+197T>C rs114825302 0.01433
NM_032380.5(GFM2):c.2212-200A>G rs16872219 0.01430
NM_032380.5(GFM2):c.-24-235C>T rs111760381 0.01142
NM_032380.5(GFM2):c.519+181G>T rs13184615 0.00984
NM_032380.5(GFM2):c.1079+310T>C rs145136703 0.00844
NM_032380.5(GFM2):c.931-67C>A rs187803936 0.00642
NM_032380.5(GFM2):c.1588-153A>G rs183986873 0.00542
NM_032380.5(GFM2):c.849+185C>T rs535593621 0.00539
NM_032380.5(GFM2):c.931-193G>A rs143133388 0.00519
NM_032380.5(GFM2):c.1511-133G>A rs550046068 0.00432
NM_032380.5(GFM2):c.2212-162C>T rs576626497 0.00399
NM_032380.5(GFM2):c.2028+330C>T rs184488832 0.00392
NM_032380.5(GFM2):c.1587+44T>A rs185670358 0.00294
NM_032380.5(GFM2):c.934C>G (p.Gln312Glu) rs116606260 0.00131
NM_032380.5(GFM2):c.979G>T (p.Val327Leu) rs150296436 0.00081
NM_032380.5(GFM2):c.777G>A (p.Lys259=) rs141864707 0.00061
NM_032380.5(GFM2):c.1321-27G>A rs183890340 0.00046
NM_032380.5(GFM2):c.1220+9A>C rs201204413 0.00024
NM_032380.5(GFM2):c.2019C>T (p.Cys673=) rs138756897 0.00016
NM_032380.5(GFM2):c.930+4A>G rs184732617 0.00016
NM_032380.5(GFM2):c.2082T>C (p.Val694=) rs375372058 0.00010
NM_032380.5(GFM2):c.1815T>C (p.Pro605=) rs201580206 0.00003
NM_032380.5(GFM2):c.2020G>A (p.Val674Met) rs367960522 0.00003
NM_032380.5(GFM2):c.431-3T>C rs369071633 0.00003
NM_032380.5(GFM2):c.609-4A>G rs368894755 0.00003
NM_032380.5(GFM2):c.850-18T>A rs545845572 0.00003
NM_032380.5(GFM2):c.282C>T (p.Ser94=) rs745682210 0.00002
NM_032380.5(GFM2):c.1359T>C (p.Ser453=) rs1554039350 0.00001
NM_032380.5(GFM2):c.1806T>A (p.Ser602=) rs369168318 0.00001
NM_032380.5(GFM2):c.87A>G (p.Arg29=) rs745476916 0.00001
NM_032380.5(GFM2):c.109C>T (p.Pro37Ser) rs138677794
NM_032380.5(GFM2):c.149-10_149-5delinsCTTTCG rs1064795248
NM_032380.5(GFM2):c.149-313G>A rs114533220
NM_032380.5(GFM2):c.1511-237C>T rs201142828
NM_032380.5(GFM2):c.390T>G (p.Phe130Leu) rs863224036
NM_032380.5(GFM2):c.450G>A (p.Leu150=) rs867915593
NM_032380.5(GFM2):c.669+7del rs768851169

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