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rs6538761

From SNPedia

Orientationplus
Stabilizedplus
Make rs6538761(A;A)
Make rs6538761(A;C)
Make rs6538761(C;C)
ReferenceGRCh38 38.1/141
Chromosome12
Position97040442
is asnp
is mentioned by
dbSNPrs6538761
dbSNP (old)rs6538761
ClinGenrs6538761
ebirs6538761
HLIrs6538761
Exacrs6538761
Varsomers6538761
Maprs6538761
PheGenIrs6538761
Biobankrs6538761
1000 genomesrs6538761
hgdprs6538761
ensemblrs6538761
gopubmedrs6538761
geneviewrs6538761
scholarrs6538761
googlers6538761
pharmgkbrs6538761
gwascentralrs6538761
openSNPrs6538761
23andMers6538761
23andMe allrs6538761
SNP Nexus

SNPshotrs6538761
SNPdbers6538761
MSV3drs6538761
GWAS Ctlgrs6538761
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 24189344]
Trait Autism
Title Common genetic variants on 1p13.2 associate with risk of autism.
Risk Allele A
P-val 2E-6
Odds Ratio 1.24 [NR]