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rs801112

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs801112(C;C)
Make rs801112(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position228860875
is asnp
is mentioned by
dbSNPrs801112
ebirs801112
HLIrs801112
Exacrs801112
Varsomers801112
Maprs801112
PheGenIrs801112
hapmaprs801112
1000 genomesrs801112
hgdprs801112
ensemblrs801112
gopubmedrs801112
geneviewrs801112
scholarrs801112
googlers801112
pharmgkbrs801112
gwascentralrs801112
openSNPrs801112
23andMers801112
23andMe allrs801112
SNP Nexus

SNPshotrs801112
SNPdbers801112
MSV3drs801112
GWAS Ctlgrs801112
GMAF0.1226
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20844546]
Trait
Title Meta-analysis of genome-wide association scans for genetic susceptibility to endometriosis in Japanese population
Risk Allele C
P-val 0.000005
Odds Ratio 1.65 [1.33-2.05]