ClinVar Miner

List of variants studied for Thrombophilia due to thrombomodulin defect by OMIM

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Total variants: 6
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HGVS dbSNP
NM_000361.2(THBD):c.-151G>T rs16984852
NM_000361.2(THBD):c.1209G>T (p.Arg403Ser) rs398122807
NM_000361.2(THBD):c.1456G>T (p.Asp486Tyr) rs41348347
THBD, -33G-A, PROMOTER
THBD, 1-BP INS, 1689T
THBD, ALA25THR

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