ClinVar Miner

List of variants in gene combination F12, SLC34A1 reported as uncertain significance for coagulation protein disease

Included ClinVar conditions (45):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
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HGVS dbSNP
NM_000505.3(F12):c.-25G>A rs886060472
NM_000505.3(F12):c.1212C>G (p.Pro404=) rs756802257
NM_000505.3(F12):c.1251-12C>A rs747726864
NM_000505.3(F12):c.158A>G (p.Tyr53Cys) rs118204455
NM_000505.3(F12):c.630C>T (p.Asp210=) rs886060471
NM_000505.3(F12):c.928A>T (p.Arg310Trp) rs749549919

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