ClinVar Miner

List of variants in gene combination FERMT1, LOC130065404 reported as benign for hereditary skin disorder

Included ClinVar conditions (790):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_017671.5(FERMT1):c.-185A>G rs2281532 0.16653

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