Have questions? Visit https://www.reddit.com/r/SNPedia

rs9640663

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;G) 0
Make rs9640663(A;A)
Make rs9640663(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position77618504
GenePTPN12
is asnp
is mentioned by
dbSNPrs9640663
ebirs9640663
HLIrs9640663
Exacrs9640663
Varsomers9640663
Maprs9640663
PheGenIrs9640663
hapmaprs9640663
1000 genomesrs9640663
hgdprs9640663
ensemblrs9640663
gopubmedrs9640663
geneviewrs9640663
scholarrs9640663
googlers9640663
pharmgkbrs9640663
gwascentralrs9640663
openSNPrs9640663
23andMers9640663
23andMe allrs9640663
SNP Nexus

SNPshotrs9640663
SNPdbers9640663
MSV3drs9640663
GWAS Ctlgrs9640663
GMAF0.2392
Max Magnitude0
? (A;A) (A;G) (G;G) 28
Venter snp
Source plos
Gene PTPN12
allele A
frequency 0.367
sift TOLERATED
HuRef 1103652618557
Disease Association Defects in PTPN12 are found in some colon cancers.



GET Evidence
PTPN12-V322I
aa_change Val322Ile
aa_change_short V322I
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.670199
summary