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rs112445441

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in complete genomics
Make rs112445441(C;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position25245347
GeneKRAS
is asnp
is mentioned by
dbSNPrs112445441
ebirs112445441
HLIrs112445441
Exacrs112445441
Varsomers112445441
Maprs112445441
PheGenIrs112445441
hapmaprs112445441
1000 genomesrs112445441
hgdprs112445441
ensemblrs112445441
gopubmedrs112445441
geneviewrs112445441
scholarrs112445441
googlers112445441
pharmgkbrs112445441
gwascentralrs112445441
openSNPrs112445441
23andMers112445441
23andMe allrs112445441
SNP Nexus

SNPshotrs112445441
SNPdbers112445441
MSV3drs112445441
GWAS Ctlgrs112445441
Max Magnitude0
OMIM190070
Desc
Variant0003
Relatedalso
ClinVar
Risk rs112445441(A,G,T;A,G,T)
Alt rs112445441(A,G,T;A,G,T)
Reference rs112445441(C;C)
Significance Pathogenic
Disease Non-small cell lung cancer Breast adenocarcinoma Juvenile myelomonocytic leukemia RAS-associated autoimmune leukoproliferative disorder
Variation info
Gene KRAS
CLNDBN Non-small cell lung cancer Breast adenocarcinoma Juvenile myelomonocytic leukemia RAS-associated autoimmune leukoproliferative disorder
Reversed 0
HGVS NC_000012.11:g.25398281C>A; NC_000012.11:g.25398281C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000038270.2, RCV000013409.6, RCV000038269.2, RCV000144967.4, RCV000144968.4,