ClinVar Miner

List of variants reported as uncertain significance for CHARGE association by Center for Human Genetics, Inc,Center for Human Genetics, Inc

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ClinVar version:
Total variants: 5
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HGVS dbSNP
NM_017780.4(CHD7):c.1397C>T (p.Ser466Leu) rs71640285
NM_017780.4(CHD7):c.3089A>C (p.Asn1030Thr) rs886041167
NM_017780.4(CHD7):c.323C>A (p.Pro108His) rs369818702
NM_017780.4(CHD7):c.712G>A (p.Val238Met) rs200898742
NM_017780.4(CHD7):c.7481C>T (p.Thr2494Ile) rs201514840

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