Have questions? Visit https://www.reddit.com/r/SNPedia

rs606231202

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs606231202(-;-)
Make rs606231202(-;TGG)
Make rs606231202(TGG;TGG)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position25245355
GeneKRAS
is asnp
is mentioned by
dbSNPrs606231202
ebirs606231202
HLIrs606231202
Exacrs606231202
Varsomers606231202
Maprs606231202
PheGenIrs606231202
hapmaprs606231202
1000 genomesrs606231202
hgdprs606231202
ensemblrs606231202
gopubmedrs606231202
geneviewrs606231202
scholarrs606231202
googlers606231202
pharmgkbrs606231202
gwascentralrs606231202
openSNPrs606231202
23andMers606231202
23andMe allrs606231202
SNP Nexus

SNPshotrs606231202
SNPdbers606231202
MSV3drs606231202
GWAS Ctlgrs606231202
Max Magnitude0
ClinVar
Risk rs606231202(TGG;TGG)
Alt rs606231202(TGG;TGG)
Reference rs606231202(;)
Significance Pathogenic
Disease Acute myeloid leukemia
Variation info
Gene KRAS
CLNDBN Acute myeloid leukemia
Reversed 1
HGVS NC_000012.11:g.25398290_25398292dupCCA
CLNSRC OMIM Allelic Variant
CLNACC RCV000013415.23,