Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs9909104
rs9909104
Entrez Id: 6470
Gene Symbol: SHMT1
SHMT1
CUI: C0018798
Disease:
Congenital Heart Defects
0.010 GeneticVariation BEFREE SSRI use was obtained from telephone interviews with mothers.<b>Results</b> For women who reported taking SSRIs periconceptionally, maternal SHMT1 (rs9909104) GG and AGgenotypes were associated with a 5.9 and 2.4 increased risk of select congenital heart defects in offspring, respectively, versus the AA genotype (BFDP=0.69). 28264803 2017