ClinVar Miner

List of variants in gene SLCO2A1 reported as uncertain significance for primary hypertrophic osteoarthropathy

Included ClinVar conditions (6):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
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HGVS dbSNP gnomAD frequency
NM_005630.3(SLCO2A1):c.484C>G (p.Pro162Ala) rs140769111 0.00130
NM_005630.3(SLCO2A1):c.1624C>T (p.Arg542Cys) rs566240756 0.00008
NM_005630.3(SLCO2A1):c.234G>A (p.Glu78=) rs545492175 0.00002
NM_005630.3(SLCO2A1):c.289C>T (p.Arg97Cys)
NM_005630.3(SLCO2A1):c.398-5T>C rs1933852686
NM_005630.3(SLCO2A1):c.659C>T (p.Ala220Val)

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