ClinVar Miner

List of variants in gene FGF3, LOC109115964 studied for auditory system disease

Included ClinVar conditions (549):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
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HGVS dbSNP
NM_005247.4(FGF3):c.100G>T (p.Gly34Cys) rs1039515359
NM_005247.4(FGF3):c.146A>G (p.Tyr49Cys) rs281860300
NM_005247.4(FGF3):c.150C>A (p.Cys50Ter) rs281860301
NM_005247.4(FGF3):c.17T>C (p.Leu6Pro) rs121917706
NM_005247.4(FGF3):c.196G>T (p.Gly66Cys) rs121917705

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