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rs2974942

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs2974942(A;G)
Make rs2974942(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position113879741
GenePPP1R3A
is asnp
is mentioned by
dbSNPrs2974942
ebirs2974942
HLIrs2974942
Exacrs2974942
Varsomers2974942
Maprs2974942
PheGenIrs2974942
hapmaprs2974942
1000 genomesrs2974942
hgdprs2974942
ensemblrs2974942
gopubmedrs2974942
geneviewrs2974942
scholarrs2974942
googlers2974942
pharmgkbrs2974942
gwascentralrs2974942
openSNPrs2974942
23andMers2974942
23andMe allrs2974942
SNP Nexus

SNPshotrs2974942
SNPdbers2974942
MSV3drs2974942
GWAS Ctlgrs2974942
GMAF0.02479
Max Magnitude0
? (A;A) (A;G) (G;G) 28
Venter snp
Source plos
Gene PPP1R3A
allele T
frequency 1
sift
HuRef 1103652678506
Disease Association Defects in PPP1R3A are a cause of insulin resistance.



Neighborrs2974944
Distance77


GET Evidence
PPP1R3A-V451M
aa_change Val451Met
aa_change_short V451M
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.969877
summary