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rs7142002

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs7142002(C;C)
Make rs7142002(C;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position101894408
GenePPP2R5C
is asnp
is mentioned by
dbSNPrs7142002
ebirs7142002
HLIrs7142002
Exacrs7142002
Varsomers7142002
Maprs7142002
PheGenIrs7142002
hapmaprs7142002
1000 genomesrs7142002
hgdprs7142002
ensemblrs7142002
gopubmedrs7142002
geneviewrs7142002
scholarrs7142002
googlers7142002
pharmgkbrs7142002
gwascentralrs7142002
openSNPrs7142002
23andMers7142002
23andMe allrs7142002
SNP Nexus

SNPshotrs7142002
SNPdbers7142002
MSV3drs7142002
GWAS Ctlgrs7142002
GMAF0.1152
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20663923OA-icon.png]
Trait Autism
Title A genomewide scan for common alleles affecting risk for autism
Risk Allele
P-val 0.000003
Odds Ratio 1.56 [1.28-1.89]