ClinVar Miner

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

Included ClinVar conditions (43):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 7
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HGVS dbSNP
NM_000505.3(F12):c.-4T>C rs1801020
NM_000505.3(F12):c.1251-9C>T rs17876032
NM_000505.3(F12):c.619G>C (p.Ala207Pro) rs17876030
NM_000505.3(F12):c.711C>T (p.Pro237=) rs17876047
NM_000505.3(F12):c.756C>T (p.Ala252=) rs41309752
NM_003052.5(SLC34A1):c.*202A>C rs6556319
NM_003052.5(SLC34A1):c.1635C>T (p.Gly545=) rs7379524

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