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rs121913236

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913236(A;A)
Make rs121913236(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position25245321
GeneKRAS
is asnp
is mentioned by
dbSNPrs121913236
dbSNP (classic)rs121913236
ClinGenrs121913236
ebirs121913236
HLIrs121913236
Exacrs121913236
Gnomadrs121913236
Varsomers121913236
LitVarrs121913236
Maprs121913236
PheGenIrs121913236
Biobankrs121913236
1000 genomesrs121913236
hgdprs121913236
ensemblrs121913236
geneviewrs121913236
scholarrs121913236
googlers121913236
pharmgkbrs121913236
gwascentralrs121913236
openSNPrs121913236
23andMers121913236
SNPshotrs121913236
SNPdbers121913236
MSV3drs121913236
GWAS Ctlgrs121913236
Max Magnitude0
ClinVar
Risk rs121913236(A;A)
Alt rs121913236(A;A)
Reference Rs121913236(C;C)
Significance Probable-Pathogenic
Disease Colorectal Neoplasms
Variation info
Gene KRAS
CLNDBN Colorectal Neoplasms
Reversed 1
HGVS NC_000012.11:g.25398255G>T
CLNSRC
CLNACC RCV000433522.1,