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rs7191700

From SNPedia

Orientationplus
Stabilizedplus
Make rs7191700(C;C)
Make rs7191700(C;T)
Make rs7191700(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position11312946
is asnp
is mentioned by
dbSNPrs7191700
ebirs7191700
HLIrs7191700
Exacrs7191700
Varsomers7191700
Maprs7191700
PheGenIrs7191700
hapmaprs7191700
1000 genomesrs7191700
hgdprs7191700
ensemblrs7191700
gopubmedrs7191700
geneviewrs7191700
scholarrs7191700
googlers7191700
pharmgkbrs7191700
gwascentralrs7191700
openSNPrs7191700
23andMers7191700
23andMe allrs7191700
SNP Nexus

SNPshotrs7191700
SNPdbers7191700
MSV3drs7191700
GWAS Ctlgrs7191700
GMAF0.2089
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22190364OA-icon.png]
Trait
Title Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci.
Risk Allele C
P-val 6E-7
Odds Ratio 1.1500 None