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rs1265883

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0
(T;T) 0 common genotype
Make rs1265883(G;G)
Make rs1265883(G;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position160495121
GeneSLAMF6
is asnp
is mentioned by
dbSNPrs1265883
dbSNP (classic)rs1265883
ClinGenrs1265883
ebirs1265883
HLIrs1265883
Exacrs1265883
Gnomadrs1265883
Varsomers1265883
LitVarrs1265883
Maprs1265883
PheGenIrs1265883
Biobankrs1265883
1000 genomesrs1265883
hgdprs1265883
ensemblrs1265883
geneviewrs1265883
scholarrs1265883
googlers1265883
pharmgkbrs1265883
gwascentralrs1265883
openSNPrs1265883
23andMers1265883
SNPshotrs1265883
SNPdbers1265883
MSV3drs1265883
GWAS Ctlgrs1265883
GMAF0.04454
Max Magnitude0
? (G;G) (G;T) (T;T) 28


GWAS snp
PMID [PMID 23612905]
Trait Graves' disease
Title Robust evidence for five new Graves' disease risk loci from a staged genome-wide association analysis.
Risk Allele C
P-val 2E-18
Odds Ratio 1.34 [1.25-1.43]