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rs12587

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs12587(A;C)
Make rs12587(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position25205894
GeneKRAS
is asnp
is mentioned by
dbSNPrs12587
dbSNP (classic)rs12587
ClinGenrs12587
ebirs12587
HLIrs12587
Exacrs12587
Gnomadrs12587
Varsomers12587
LitVarrs12587
Maprs12587
PheGenIrs12587
Biobankrs12587
1000 genomesrs12587
hgdprs12587
ensemblrs12587
geneviewrs12587
scholarrs12587
googlers12587
pharmgkbrs12587
gwascentralrs12587
openSNPrs12587
23andMers12587
SNPshotrs12587
SNPdbers12587
MSV3drs12587
GWAS Ctlgrs12587
Max Magnitude0
? (A;A) (A;C) (C;C) 28


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


ClinVar
Risk rs12587(C;C)
Alt rs12587(C;C)
Reference Rs12587(A;A)
Significance Probable-non-pathogenic
Disease Cardio-facio-cutaneous syndrome Noonan syndrome
Variation info
Gene KRAS
CLNDBN Cardio-facio-cutaneous syndrome Noonan syndrome
Reversed 1
HGVS NC_000012.11:g.25358828T>G
CLNSRC
CLNACC RCV000282245.1, RCV000401125.1,



[PMID 33152124] Common gene variants within 3'-untranslated regions as modulators of multiple myeloma risk and survival.