ClinVar Miner

List of variants in gene F13B reported as benign for congenital factor XIII deficiency

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 4
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NM_001994.2(F13B):c.*143G>A rs698859
NM_001994.2(F13B):c.1806T>C (p.Asn602=) rs5998
NM_001994.2(F13B):c.344G>A (p.Arg115His) rs6003
NM_001994.2(F13B):c.456A>G (p.Thr152=) rs5997

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