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rs975730

From SNPedia

Orientationminus
Stabilizedminus
Make rs975730(C;C)
Make rs975730(C;T)
Make rs975730(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position128303768
is asnp
is mentioned by
dbSNPrs975730
dbSNP (classic)rs975730
ClinGenrs975730
ebirs975730
HLIrs975730
Exacrs975730
Gnomadrs975730
Varsomers975730
LitVarrs975730
Maprs975730
PheGenIrs975730
Biobankrs975730
1000 genomesrs975730
hgdprs975730
ensemblrs975730
geneviewrs975730
scholarrs975730
googlers975730
pharmgkbrs975730
gwascentralrs975730
openSNPrs975730
23andMers975730
SNPshotrs975730
SNPdbers975730
MSV3drs975730
GWAS Ctlgrs975730
GMAF0.4743
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 21383967OA-icon.png]
Trait
Title Meta-Analysis of Genome-Wide Association Studies in Celiac Disease and Rheumatoid Arthritis Identifies Fourteen Non-HLA Shared Loci
Risk Allele
P-val 2E-8
Odds Ratio None None