Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs763351020
rs763351020
SERPINE1
CUI: C0242342
Disease: Sheehan Syndrome
Sheehan Syndrome 		0.010 GeneticVariation BEFREE We suggest that the genetic mutations of FV-Leiden, FII G20210A, MTHFR C677T, MTHFR A1298C and PAI-1 4G/5G increase the risk of SS. 21107737

2011