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rs121434623

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121434623(A;G)
Make rs121434623(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position77571160
GenePTPN12
is asnp
is mentioned by
dbSNPrs121434623
ebirs121434623
HLIrs121434623
Exacrs121434623
Varsomers121434623
Maprs121434623
PheGenIrs121434623
hapmaprs121434623
1000 genomesrs121434623
hgdprs121434623
ensemblrs121434623
gopubmedrs121434623
geneviewrs121434623
scholarrs121434623
googlers121434623
pharmgkbrs121434623
gwascentralrs121434623
openSNPrs121434623
23andMers121434623
23andMe allrs121434623
SNP Nexus

SNPshotrs121434623
SNPdbers121434623
MSV3drs121434623
GWAS Ctlgrs121434623
Max Magnitude0
OMIM600079
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121434623(G;G)
Alt rs121434623(G;G)
Reference rs121434623(A;A)
Significance Pathogenic
Disease Carcinoma of colon
Variation info
Gene PTPN12
CLNDBN Carcinoma of colon
Reversed 0
HGVS NC_000007.13:g.77200477A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010055.8,