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rs4916321

From SNPedia

Orientationplus
Stabilizedplus
Make rs4916321(G;G)
Make rs4916321(G;T)
Make rs4916321(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position173315060
GeneIGHVII-15-1
is asnp
is mentioned by
dbSNPrs4916321
ebirs4916321
HLIrs4916321
Exacrs4916321
Varsomers4916321
Maprs4916321
PheGenIrs4916321
hapmaprs4916321
1000 genomesrs4916321
hgdprs4916321
ensemblrs4916321
gopubmedrs4916321
geneviewrs4916321
scholarrs4916321
googlers4916321
pharmgkbrs4916321
gwascentralrs4916321
openSNPrs4916321
23andMers4916321
23andMe allrs4916321
SNP Nexus

SNPshotrs4916321
SNPdbers4916321
MSV3drs4916321
GWAS Ctlgrs4916321
GMAF0.06336
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 23412934OA-icon.png]
Trait Multiple sclerosis
Title A genome-wide association study of brain lesion distribution in multiple sclerosis.
Risk Allele
P-val 7E-6
Odds Ratio NR NR