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rs121913535

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913535(G;T)
Make rs121913535(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position25245348
GeneKRAS
is asnp
is mentioned by
dbSNPrs121913535
ebirs121913535
HLIrs121913535
Exacrs121913535
Varsomers121913535
Maprs121913535
PheGenIrs121913535
hapmaprs121913535
1000 genomesrs121913535
hgdprs121913535
ensemblrs121913535
gopubmedrs121913535
geneviewrs121913535
scholarrs121913535
googlers121913535
pharmgkbrs121913535
gwascentralrs121913535
openSNPrs121913535
23andMers121913535
23andMe allrs121913535
SNP Nexus

SNPshotrs121913535
SNPdbers121913535
MSV3drs121913535
GWAS Ctlgrs121913535
Max Magnitude0
OMIM190070
Desc
Variant0016
Relatedalso
ClinVar
Risk rs121913535(A,C,T;A,C,T)
Alt rs121913535(A,C,T;A,C,T)
Reference rs121913535(G;G)
Significance Pathogenic
Disease Non-small cell lung cancer RAS-associated autoimmune leukoproliferative disorder Pilocytic astrocytoma
Variation info
Gene KRAS
CLNDBN Non-small cell lung cancer RAS-associated autoimmune leukoproliferative disorder Pilocytic astrocytoma
Reversed 1
HGVS NC_000012.11:g.25398282C>A; NC_000012.11:g.25398282C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000038268.2, RCV000144972.3, RCV000013424.4, RCV000038267.2,