ClinVar Miner

List of variants in gene F11 reported as benign 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_000128.3(F11):c.*296G>C rs4253430
NM_000128.3(F11):c.*479A>T rs1062547
NM_000128.3(F11):c.*852G>A rs4253431
NM_000128.3(F11):c.-316C>G rs3733403
NM_000128.3(F11):c.1191T>C (p.Gly397=) rs5970
NM_000128.3(F11):c.801A>G (p.Thr267=) rs5974

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