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rs10136766

From SNPedia

Orientationplus
Stabilizedplus
Make rs10136766(A;A)
Make rs10136766(A;G)
Make rs10136766(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position105766248
GeneIGH@
is asnp
is mentioned by
dbSNPrs10136766
ebirs10136766
HLIrs10136766
Exacrs10136766
Varsomers10136766
Maprs10136766
PheGenIrs10136766
hapmaprs10136766
1000 genomesrs10136766
hgdprs10136766
ensemblrs10136766
gopubmedrs10136766
geneviewrs10136766
scholarrs10136766
googlers10136766
pharmgkbrs10136766
gwascentralrs10136766
openSNPrs10136766
23andMers10136766
23andMe allrs10136766
SNP Nexus

SNPshotrs10136766
SNPdbers10136766
MSV3drs10136766
GWAS Ctlgrs10136766
GMAF0.2897
Max Magnitude
GWAS snp
PMID [PMID 23225573OA-icon.png]
Trait IgG levels
Title Genetic variants in the immunoglobulin heavy chain locus are associated with the IgG index in multiple sclerosis.
Risk Allele A
P-val 8E-16
Odds Ratio .23 [NR] unit increase