ClinVar Miner

List of variants reported as uncertain significance for Smith-Lemli-Opitz syndrome by Fulgent Genetics,Fulgent Genetics

Included ClinVar conditions (1):
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Total variants: 7
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HGVS dbSNP
NM_001360.2(DHCR7):c.1091C>T (p.Thr364Met) rs567600444
NM_001360.2(DHCR7):c.1370G>A (p.Arg457Gln) rs886043122
NM_001360.2(DHCR7):c.223A>T (p.Ile75Phe) rs370748173
NM_001360.2(DHCR7):c.400G>T (p.Val134Leu) rs201466849
NM_001360.2(DHCR7):c.682C>T (p.Arg228Trp) rs775773057
NM_001360.2(DHCR7):c.719A>G (p.Asn240Ser) rs148609143
NM_001360.2(DHCR7):c.988G>A (p.Val330Met) rs139724817

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