Have questions? Visit https://www.reddit.com/r/SNPedia

rs9909104

From SNPedia

Orientationplus
Stabilizedplus
Make rs9909104(C;C)
Make rs9909104(C;T)
Make rs9909104(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position18344707
GeneSHMT1
is asnp
is mentioned by
dbSNPrs9909104
ebirs9909104
HLIrs9909104
Exacrs9909104
Varsomers9909104
Maprs9909104
PheGenIrs9909104
hapmaprs9909104
1000 genomesrs9909104
hgdprs9909104
ensemblrs9909104
gopubmedrs9909104
geneviewrs9909104
scholarrs9909104
googlers9909104
pharmgkbrs9909104
gwascentralrs9909104
openSNPrs9909104
23andMers9909104
23andMe allrs9909104
SNP Nexus

SNPshotrs9909104
SNPdbers9909104
MSV3drs9909104
GWAS Ctlgrs9909104
GMAF0.3122
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 18381459OA-icon.png] 829 Caucasian cases with primary epithelial ovarian cancer and 941 frequency-matched unaffected controls
  • Each copy of the minor allele in SHMT1 intron 5 A>G (rs9909104) was associated with epithelial ovarian cancer [odds ratio (OR), 1.2; 95% confidence interval (95% CI), 1.0-1.4; P trend = 0.02; FPRP = 0.16] and a 5-SNP SHMT1 haplotype was associated with decreased risk (P = 0.01; FPRP = 0.09).


[PMID 23940529OA-icon.png] Roles of genetic polymorphisms in the folate pathway in childhood acute lymphoblastic leukemia evaluated by bayesian relevance and effect size analysis