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rs121913530

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913530(G;T)
Make rs121913530(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position25245351
GeneKRAS
is asnp
is mentioned by
dbSNPrs121913530
ebirs121913530
HLIrs121913530
Exacrs121913530
Varsomers121913530
Maprs121913530
PheGenIrs121913530
hapmaprs121913530
1000 genomesrs121913530
hgdprs121913530
ensemblrs121913530
gopubmedrs121913530
geneviewrs121913530
scholarrs121913530
googlers121913530
pharmgkbrs121913530
gwascentralrs121913530
openSNPrs121913530
23andMers121913530
23andMe allrs121913530
SNP Nexus

SNPshotrs121913530
SNPdbers121913530
MSV3drs121913530
GWAS Ctlgrs121913530
Max Magnitude0
OMIM190070
Desc
Variant0001
Relatedalso
OMIM190070
Desc
Variant0002
Relatedalso
OMIM190070
Desc
Variant0007
Relatedalso
OMIM608089
Desc
Variant
Relatedalso
OMIM167000
Desc
Variant
Relatedalso
ClinVar
Risk rs121913530(A,C,T;A,C,T)
Alt rs121913530(A,C,T;A,C,T)
Reference rs121913530(G;G)
Significance Pathogenic
Disease Lung cancer Non-small cell lung cancer Endometrial carcinoma Squamous cell carcinoma of lung Malignant tumor of urinary bladder Neoplasm of stomach Neoplasm of ovary Juvenile myelomonocytic leukemia
Variation info
Gene KRAS
CLNDBN Lung cancer Non-small cell lung cancer Endometrial carcinoma Squamous cell carcinoma of lung Malignant tumor of urinary bladder Neoplasm of stomach Neoplasm of ovary Juvenile myelomonocytic leukemia
Reversed 1
HGVS NC_000012.11:g.25398285C>A; NC_000012.11:g.25398285C>G; NC_000012.11:g.25398285C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013406.4, RCV000038265.2, RCV000119791.1, RCV000013407.4, RCV000013408.4, RCV000154401.2, RCV000013414.5, RCV000038264.2, RCV000119790.1, RCV000144971.3,