ClinVar Miner

List of variants in gene SGCA reported as likely benign for not provided

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Gene type:
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Total variants: 24
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HGVS dbSNP gnomAD frequency
NM_000023.4(SGCA):c.386-166G>A rs11870423 0.03655
NM_000023.4(SGCA):c.37+290G>A rs73987434 0.01040
NM_000023.4(SGCA):c.38-96C>T rs148431038 0.00865
NM_000023.4(SGCA):c.984-165C>T rs143663300 0.00808
NM_000023.4(SGCA):c.984-100A>G rs116638508 0.00799
NC_000017.11:g.50165951C>A rs75145501 0.00730
NM_000023.4(SGCA):c.983+56C>A rs147162020 0.00629
NM_000023.4(SGCA):c.584+162C>T rs190245746 0.00395
NM_000023.4(SGCA):c.158-11G>A rs140261054 0.00157
NM_000023.4(SGCA):c.329G>A (p.Arg110Gln) rs145697858 0.00087
NM_000023.4(SGCA):c.366G>A (p.Leu122=) rs147739328 0.00075
NM_000023.4(SGCA):c.690G>C (p.Leu230=) rs139454982 0.00049
NM_000023.4(SGCA):c.662G>A (p.Arg221His) rs138254713 0.00027
NM_000023.4(SGCA):c.408C>T (p.Ala136=) rs143551687 0.00013
NM_000023.4(SGCA):c.270C>T (p.Tyr90=) rs749205073 0.00004
NM_000023.4(SGCA):c.158-4C>A rs776411719 0.00003
NM_000023.4(SGCA):c.1131C>T (p.Ser377=) rs769951787 0.00001
NM_000023.4(SGCA):c.327T>C (p.Asn109=) rs752288242 0.00001
NM_000023.4(SGCA):c.1080G>T (p.Leu360=) rs1598277856
NM_000023.4(SGCA):c.201G>A (p.Gln67=)
NM_000023.4(SGCA):c.38-46G>C rs142537375
NM_000023.4(SGCA):c.584+156G>A rs56273576
NM_000023.4(SGCA):c.600G>C (p.Val200=) rs764188161
NM_000023.4(SGCA):c.956+7G>A rs1598270831

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