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rs4703129

From SNPedia

Orientationplus
Stabilizedplus
Make rs4703129(A;A)
Make rs4703129(A;C)
Make rs4703129(C;C)
ReferenceGRCh38 38.1/141
Chromosome5
Position98553032
is asnp
is mentioned by
dbSNPrs4703129
ebirs4703129
HLIrs4703129
Exacrs4703129
Varsomers4703129
Maprs4703129
PheGenIrs4703129
hapmaprs4703129
1000 genomesrs4703129
hgdprs4703129
ensemblrs4703129
gopubmedrs4703129
geneviewrs4703129
scholarrs4703129
googlers4703129
pharmgkbrs4703129
gwascentralrs4703129
openSNPrs4703129
23andMers4703129
23andMe allrs4703129
SNP Nexus

SNPshotrs4703129
SNPdbers4703129
MSV3drs4703129
GWAS Ctlgrs4703129
GMAF0.3985
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 21182207OA-icon.png]
Trait
Title Variants in several genomic regions associated with Asperger disorder
Risk Allele
P-val 0.000001
Odds Ratio None None