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rs1137282

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1137282(C;C)
Make rs1137282(C;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position25209843
GeneKRAS
is asnp
is mentioned by
dbSNPrs1137282
ebirs1137282
HLIrs1137282
Exacrs1137282
Varsomers1137282
Maprs1137282
PheGenIrs1137282
hapmaprs1137282
1000 genomesrs1137282
hgdprs1137282
ensemblrs1137282
gopubmedrs1137282
geneviewrs1137282
scholarrs1137282
googlers1137282
pharmgkbrs1137282
gwascentralrs1137282
openSNPrs1137282
23andMers1137282
23andMe allrs1137282
SNP Nexus

SNPshotrs1137282
SNPdbers1137282
MSV3drs1137282
GWAS Ctlgrs1137282
GMAF0.1657
Max Magnitude0

[PMID 21688344] Effects of KRAS mutation and polymorphism on the risk and prognosis of oral squamous cell carcinoma

? (A;A) (A;G) (G;G)
[PMID 18805939OA-icon.png] Functional genetic polymorphisms and female reproductive disorders: part II--endometriosis.


ClinVar
Risk rs1137282(C;C)
Alt rs1137282(C;C)
Reference rs1137282(T;T)
Significance Non-pathogenic
Disease not specified
Variation info
Gene KRAS
CLNDBN not specified
Reversed 1
HGVS NC_000012.11:g.25362777A>G
CLNSRC ClinVar GeneDx
CLNACC RCV000038277.8,



[PMID 26515332] KRAS polymorphisms are associated with survival of CRC in Chinese population