ClinVar Miner

List of variants in gene combination GH-LCR, SCN4A reported as likely benign by GeneDx

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Gene type:
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Total variants: 44
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HGVS dbSNP
NM_000334.4(SCN4A):c.2055G>A (p.Thr685=) rs766227475
NM_000334.4(SCN4A):c.2130C>T (p.Ile710=) rs776552053
NM_000334.4(SCN4A):c.2223C>T (p.Arg741=) rs1041781133
NM_000334.4(SCN4A):c.2377-17delC rs761358378
NM_000334.4(SCN4A):c.2386C>T (p.Leu796=) rs750053946
NM_000334.4(SCN4A):c.2421C>T (p.Ala807=) rs540328974
NM_000334.4(SCN4A):c.2448T>C (p.Asp816=) rs150307926
NM_000334.4(SCN4A):c.2478C>T (p.Ile826=) rs371914255
NM_000334.4(SCN4A):c.2574C>T (p.Leu858=) rs184107335
NM_000334.4(SCN4A):c.2623C>T (p.Pro875Ser) rs201148948
NM_000334.4(SCN4A):c.2697G>A (p.Leu899=) rs199827271
NM_000334.4(SCN4A):c.2748C>G (p.Asn916Lys) rs115379510
NM_000334.4(SCN4A):c.2778C>T (p.Ile926=)
NM_000334.4(SCN4A):c.2854-5C>T rs374039266
NM_000334.4(SCN4A):c.2861C>T (p.Pro954Leu) rs201367621
NM_000334.4(SCN4A):c.2889C>A (p.Ser963=) rs757881584
NM_000334.4(SCN4A):c.2955C>T (p.Pro985=) rs375621334
NM_000334.4(SCN4A):c.3285C>T (p.Asn1095=)
NM_000334.4(SCN4A):c.3288C>T (p.Ala1096=)
NM_000334.4(SCN4A):c.3312C>T (p.Ile1104=) rs779189351
NM_000334.4(SCN4A):c.3429C>T (p.Phe1143=) rs373597946
NM_000334.4(SCN4A):c.3441+4G>A rs765176007
NM_000334.4(SCN4A):c.3442-18G>T rs377676692
NM_000334.4(SCN4A):c.3465C>T (p.Gly1155=) rs566581547
NM_000334.4(SCN4A):c.3576C>T (p.Thr1192=)
NM_000334.4(SCN4A):c.3774+7C>T rs199659791
NM_000334.4(SCN4A):c.3774+9G>A
NM_000334.4(SCN4A):c.3912+277G>A
NM_000334.4(SCN4A):c.3912+91G>A
NM_000334.4(SCN4A):c.3963C>T (p.Asn1321=) rs747602881
NM_000334.4(SCN4A):c.4018-222A>T
NM_000334.4(SCN4A):c.4215C>T (p.Leu1405=) rs141215137
NM_000334.4(SCN4A):c.4359G>A (p.Ala1453=) rs757915411
NM_000334.4(SCN4A):c.4360C>A (p.Arg1454=) rs879253789
NM_000334.4(SCN4A):c.4410G>A (p.Thr1470=) rs534861830
NM_000334.4(SCN4A):c.4605G>A (p.Ser1535=) rs182438287
NM_000334.4(SCN4A):c.4680G>A (p.Pro1560=) rs370207597
NM_000334.4(SCN4A):c.4690G>A (p.Val1564Ile) rs202106192
NM_000334.4(SCN4A):c.5124C>T (p.Ala1708=) rs1555600600
NM_000334.4(SCN4A):c.5181G>A (p.Glu1727=) rs368263333
NM_000334.4(SCN4A):c.5190C>T (p.Cys1730=) rs113277954
NM_000334.4(SCN4A):c.5277C>T (p.Asp1759=) rs548333586
NM_000334.4(SCN4A):c.5343C>T (p.Gly1781=) rs745441690
NM_000334.4(SCN4A):c.5468C>G (p.Pro1823Arg) rs376833596

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