ClinVar Miner

List of variants in gene combination GLA, RPL36A-HNRNPH2 reported as likely benign for not specified

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Total variants: 35
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HGVS dbSNP
NM_000169.2(GLA):c.-13G>C rs782051708
NM_000169.2(GLA):c.-32G>A rs1057523740
NM_000169.2(GLA):c.-44C>G rs781906252
NM_000169.2(GLA):c.1000-14T>C rs397515868
NM_000169.2(GLA):c.1008C>T (p.Asn336=) rs901454780
NM_000169.2(GLA):c.1095T>C (p.Tyr365=) rs104894849
NM_000169.2(GLA):c.1102G>A (p.Ala368Thr) rs144994244
NM_000169.2(GLA):c.1102G>C (p.Ala368Pro) rs144994244
NM_000169.2(GLA):c.1153A>G (p.Thr385Ala) rs397515869
NM_000169.2(GLA):c.1191T>C (p.Tyr397=) rs869312236
NM_000169.2(GLA):c.1261A>G (p.Met421Val) rs144060196
NM_000169.2(GLA):c.129C>T (p.Gly43=) rs146177035
NM_000169.2(GLA):c.133C>T (p.Leu45=) rs143084761
NM_000169.2(GLA):c.194+14G>C rs876657469
NM_000169.2(GLA):c.196G>C (p.Glu66Gln) rs104894833
NM_000169.2(GLA):c.28C>T (p.Leu10=) rs727503073
NM_000169.2(GLA):c.320A>G (p.Gln107Arg) rs727505060
NM_000169.2(GLA):c.345T>C (p.His115=) rs782260908
NM_000169.2(GLA):c.376A>G (p.Ser126Gly) rs149391489
NM_000169.2(GLA):c.416A>G (p.Asn139Ser) rs138886989
NM_000169.2(GLA):c.48T>G (p.Leu16=) rs201449986
NM_000169.2(GLA):c.501A>T (p.Leu167=) rs782486830
NM_000169.2(GLA):c.630C>T (p.Pro210=) rs727503071
NM_000169.2(GLA):c.639+6A>C rs200096940
NM_000169.2(GLA):c.640-731G>A rs2473815
NM_000169.2(GLA):c.6G>A (p.Gln2=) rs782748047
NM_000169.2(GLA):c.714T>C (p.Ser238=) rs397515872
NM_000169.2(GLA):c.721A>G (p.Ser241Gly) rs730880438
NM_000169.2(GLA):c.801+14C>T rs200744672
NM_000169.2(GLA):c.8T>C (p.Leu3Pro) rs150547672
NM_000169.2(GLA):c.937G>T (p.Asp313Tyr) rs28935490
NM_000169.2(GLA):c.945C>T (p.Asp315=) rs151208856
NM_000169.2(GLA):c.978G>A (p.Lys326=) rs151195362
NM_000169.2(GLA):c.984G>T (p.Gly328=) rs376623208
NM_000169.2(GLA):c.991C>T (p.Leu331Phe) rs730880437

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