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

rs121912661

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121912661(G;T)
Make rs121912661(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position7676264
GeneTP53
is asnp
is mentioned by
dbSNPrs121912661
ebirs121912661
HLIrs121912661
Exacrs121912661
Varsomers121912661
Maprs121912661
PheGenIrs121912661
hapmaprs121912661
1000 genomesrs121912661
hgdprs121912661
ensemblrs121912661
gopubmedrs121912661
geneviewrs121912661
scholarrs121912661
googlers121912661
pharmgkbrs121912661
gwascentralrs121912661
openSNPrs121912661
23andMers121912661
23andMe allrs121912661
SNP Nexus

SNPshotrs121912661
SNPdbers121912661
MSV3drs121912661
GWAS Ctlgrs121912661
Max Magnitude0
OMIM191170
Desc
Variant0027
Relatedalso
ClinVar
Risk rs121912661(C,T;C,T)
Alt rs121912661(C,T;C,T)
Reference rs121912661(G;G)
Significance Pathogenic
Disease Carcinoma of pancreas Hereditary cancer-predisposing syndrome
Variation info
Gene TP53
CLNDBN Carcinoma of pancreas Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.7579582C>A; NC_000017.10:g.7579582C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000013170.4, RCV000131759.2,