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rs4961252

From SNPedia

Orientationplus
Stabilizedplus
Make rs4961252(A;A)
Make rs4961252(A;G)
Make rs4961252(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position141094845
is asnp
is mentioned by
dbSNPrs4961252
dbSNP (classic)rs4961252
ClinGenrs4961252
ebirs4961252
HLIrs4961252
Exacrs4961252
Gnomadrs4961252
Varsomers4961252
LitVarrs4961252
Maprs4961252
PheGenIrs4961252
Biobankrs4961252
1000 genomesrs4961252
hgdprs4961252
ensemblrs4961252
geneviewrs4961252
scholarrs4961252
googlers4961252
pharmgkbrs4961252
gwascentralrs4961252
openSNPrs4961252
23andMers4961252
SNPshotrs4961252
SNPdbers4961252
MSV3drs4961252
GWAS Ctlgrs4961252
GMAF0.4449
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 21502966]
Trait
Title Single-nucleotide polymorphisms in HLA- and non-HLA genes associated with the development of antibodies to interferon-β therapy in multiple sclerosis patients.
Risk Allele G
P-val 3E-8
Odds Ratio 0.2300 [NR] unit increase