ClinVar Miner

List of variants in gene GFM2 reported as uncertain significance by GeneDx

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Gene type:
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Total variants: 30
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HGVS dbSNP gnomAD frequency
NM_032380.5(GFM2):c.1234C>T (p.Arg412Cys) rs142425196 0.00149
NM_032380.5(GFM2):c.1728T>A (p.Asp576Glu) rs140077535 0.00104
NM_032380.5(GFM2):c.1424C>T (p.Ala475Val) rs142986380 0.00098
NM_032380.5(GFM2):c.1984T>A (p.Ser662Thr) rs141789665 0.00084
NM_032380.5(GFM2):c.2213G>A (p.Gly738Asp) rs139901493 0.00032
NM_032380.5(GFM2):c.1070A>G (p.Tyr357Cys) rs138670775 0.00029
NM_032380.5(GFM2):c.1147C>G (p.Leu383Val) rs199681606 0.00019
NM_032380.5(GFM2):c.1040T>C (p.Met347Thr) rs774464063 0.00017
NM_032380.5(GFM2):c.2231G>A (p.Arg744Gln) rs151093565 0.00012
NM_032380.5(GFM2):c.277T>C (p.Tyr93His) rs863224038 0.00009
NM_032380.5(GFM2):c.1196T>C (p.Ile399Thr) rs143233751 0.00007
NM_032380.5(GFM2):c.1376G>A (p.Arg459His) rs769129792 0.00004
NM_032380.5(GFM2):c.1387C>T (p.Arg463Trp) rs377321462 0.00003
NM_032380.5(GFM2):c.1523C>T (p.Ala508Val) rs747081870 0.00002
NM_032380.5(GFM2):c.2287A>G (p.Met763Val) rs182739367 0.00002
NM_032380.5(GFM2):c.1127A>G (p.His376Arg) rs1162619865 0.00001
NM_032380.5(GFM2):c.1229T>A (p.Ile410Lys) rs863224037 0.00001
NM_032380.5(GFM2):c.542G>A (p.Arg181Lys) rs150612355 0.00001
NM_032380.5(GFM2):c.1247C>T (p.Pro416Leu)
NM_032380.5(GFM2):c.1268A>C (p.Glu423Ala)
NM_032380.5(GFM2):c.1384G>A (p.Glu462Lys) rs145221708
NM_032380.5(GFM2):c.1541G>C (p.Arg514Pro) rs755301816
NM_032380.5(GFM2):c.1588A>G (p.Thr530Ala)
NM_032380.5(GFM2):c.1615C>T (p.His539Tyr)
NM_032380.5(GFM2):c.1732T>A (p.Leu578Ile)
NM_032380.5(GFM2):c.1843A>G (p.Ile615Val)
NM_032380.5(GFM2):c.2132del (p.Arg711fs) rs1167646213
NM_032380.5(GFM2):c.2152del (p.Ile718fs)
NM_032380.5(GFM2):c.2219C>T (p.Ser740Leu)
NM_032380.5(GFM2):c.564A>G (p.Ile188Met)

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