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rs4675502

From SNPedia

Orientationplus
Stabilizedplus
Make rs4675502(A;A)
Make rs4675502(A;G)
Make rs4675502(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position205221447
GenePARD3B
is asnp
is mentioned by
dbSNPrs4675502
ebirs4675502
HLIrs4675502
Exacrs4675502
Varsomers4675502
Maprs4675502
PheGenIrs4675502
hapmaprs4675502
1000 genomesrs4675502
hgdprs4675502
ensemblrs4675502
gopubmedrs4675502
geneviewrs4675502
scholarrs4675502
googlers4675502
pharmgkbrs4675502
gwascentralrs4675502
openSNPrs4675502
23andMers4675502
23andMe allrs4675502
SNP Nexus

SNPshotrs4675502
SNPdbers4675502
MSV3drs4675502
GWAS Ctlgrs4675502
GMAF0.433
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 4E-7
Odds Ratio 1.28 [1.16-1.41]