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rs7779014

From SNPedia

Orientationplus
Stabilizedplus
Make rs7779014(C;C)
Make rs7779014(C;T)
Make rs7779014(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position76346269
GeneYWHAG
is asnp
is mentioned by
dbSNPrs7779014
ebirs7779014
HLIrs7779014
Exacrs7779014
Varsomers7779014
Maprs7779014
PheGenIrs7779014
hapmaprs7779014
1000 genomesrs7779014
hgdprs7779014
ensemblrs7779014
gopubmedrs7779014
geneviewrs7779014
scholarrs7779014
googlers7779014
pharmgkbrs7779014
gwascentralrs7779014
openSNPrs7779014
23andMers7779014
23andMe allrs7779014
SNP Nexus

SNPshotrs7779014
SNPdbers7779014
MSV3drs7779014
GWAS Ctlgrs7779014
GMAF0.3398
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21654844OA-icon.png]
Trait
Title Genome-wide association study of severity in multiple sclerosis.
Risk Allele T
P-val 0.000008
Odds Ratio 0.4800 [NR] unit increase