ClinVar Miner

List of variants in gene LRP6 studied for coronary artery disease, autosomal dominant 2

Included ClinVar conditions (2):
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Gene type:
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Total variants: 9
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HGVS dbSNP gnomAD frequency
NM_002336.3(LRP6):c.2382C>T (p.Asn794=) rs74774620 0.00556
NM_002336.3(LRP6):c.3192A>G (p.Val1064=) rs114714311 0.00552
NM_002336.3(LRP6):c.2203G>A (p.Asp735Asn) rs149258721 0.00026
NM_002336.3(LRP6):c.1079G>A (p.Arg360His) rs141212743 0.00013
NM_002336.3(LRP6):c.1298A>G (p.Asn433Ser) rs397515473 0.00002
NM_002336.3(LRP6):c.1418G>A (p.Arg473Gln) rs397515474 0.00002
NM_002336.3(LRP6):c.1831C>T (p.Arg611Cys) rs121918313 0.00002
NM_002336.3(LRP6):c.1118A>G (p.Tyr373Cys) rs1178632796 0.00001
NM_002336.3(LRP6):c.2218C>T (p.Gln740Ter) rs1591901585

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