ClinVar Miner

List of variants in gene LOC129932084, NCF2 studied for hematologic disorder

Included ClinVar conditions (819):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 3
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HGVS dbSNP gnomAD frequency
NM_000433.3(NCF2):c.-240T>G rs2274065 0.19754
NM_000433.3(NCF2):c.-249_-248insA rs35066000 0.06127
NM_000433.3(NCF2):c.-264C>T rs150182900 0.00009

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