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rs121913238

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913238(C;G)
Make rs121913238(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position25227343
GeneKRAS
is asnp
is mentioned by
dbSNPrs121913238
dbSNP (classic)rs121913238
ClinGenrs121913238
ebirs121913238
HLIrs121913238
Exacrs121913238
Gnomadrs121913238
Varsomers121913238
LitVarrs121913238
Maprs121913238
PheGenIrs121913238
Biobankrs121913238
1000 genomesrs121913238
hgdprs121913238
ensemblrs121913238
geneviewrs121913238
scholarrs121913238
googlers121913238
pharmgkbrs121913238
gwascentralrs121913238
openSNPrs121913238
23andMers121913238
SNPshotrs121913238
SNPdbers121913238
MSV3drs121913238
GWAS Ctlgrs121913238
Max Magnitude0
ClinVar
Risk rs121913238(A;A) rs121913238(G;G)
Alt rs121913238(A;A) rs121913238(G;G)
Reference Rs121913238(C;C)
Significance Pathogenic
Disease Colorectal Neoplasms Non-small cell lung cancer Neoplasm of the thyroid gland
Variation info
Gene KRAS
CLNDBN Colorectal Neoplasms Non-small cell lung cancer Neoplasm of the thyroid gland
Reversed 1
HGVS NC_000012.11:g.25380277G>C; NC_000012.11:g.25380277G>T
CLNSRC COSMIC
CLNACC RCV000422828.1, RCV000154402.3, RCV000423236.1, RCV000440889.1,