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rs7711337

From SNPedia

Orientationplus
Stabilizedplus
Make rs7711337(A;A)
Make rs7711337(A;G)
Make rs7711337(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position162656512
is asnp
is mentioned by
dbSNPrs7711337
ebirs7711337
HLIrs7711337
Exacrs7711337
Varsomers7711337
Maprs7711337
PheGenIrs7711337
hapmaprs7711337
1000 genomesrs7711337
hgdprs7711337
ensemblrs7711337
gopubmedrs7711337
geneviewrs7711337
scholarrs7711337
googlers7711337
pharmgkbrs7711337
gwascentralrs7711337
openSNPrs7711337
23andMers7711337
23andMe allrs7711337
SNP Nexus

SNPshotrs7711337
SNPdbers7711337
MSV3drs7711337
GWAS Ctlgrs7711337
GMAF0.3402
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 22843504OA-icon.png]
Trait Autism
Title Individual common variants exert weak effects on the risk for autism spectrum disorderspi.
Risk Allele
P-val 8E-7
Odds Ratio 1.22 [1.12-1.32]