ClinVar Miner

List of variants studied for familial apolipoprotein C-II deficiency by New York Genome Center

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 3
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HGVS dbSNP gnomAD frequency
NM_000483.5(APOC2):c.85G>A (p.Asp29Asn) rs147242592 0.00076
NM_000483.5(APOC2):c.122A>C (p.Lys41Thr) rs120074114 0.00071
NM_000483.5(APOC2):c.-14+8A>G

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