ClinVar Miner

List of variants in gene CCNF, LOC105371050 studied for amyotrophic lateral sclerosis

Included ClinVar conditions (70):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 2
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HGVS dbSNP gnomAD frequency
NM_001761.3(CCNF):c.1870G>A (p.Glu624Lys) rs771621178 0.00002
NM_001761.3(CCNF):c.1918G>A (p.Val640Met) rs373872375 0.00001

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