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rs730880472

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880472(G;G)
Make rs730880472(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position25245317
GeneKRAS
is asnp
is mentioned by
dbSNPrs730880472
ebirs730880472
HLIrs730880472
Exacrs730880472
Varsomers730880472
Maprs730880472
PheGenIrs730880472
hapmaprs730880472
1000 genomesrs730880472
hgdprs730880472
ensemblrs730880472
gopubmedrs730880472
geneviewrs730880472
scholarrs730880472
googlers730880472
pharmgkbrs730880472
gwascentralrs730880472
openSNPrs730880472
23andMers730880472
23andMe allrs730880472
SNP Nexus

SNPshotrs730880472
SNPdbers730880472
MSV3drs730880472
GWAS Ctlgrs730880472
Max Magnitude0
ClinVar
Risk rs730880472(G;G)
Alt rs730880472(G;G)
Reference rs730880472(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KRAS
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.25398251A>C
CLNSRC
CLNACC RCV000157948.1,