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

rs727503109

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs727503109(A;G)
Make rs727503109(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position25245277
GeneKRAS
is asnp
is mentioned by
dbSNPrs727503109
ebirs727503109
HLIrs727503109
Exacrs727503109
Varsomers727503109
Maprs727503109
PheGenIrs727503109
hapmaprs727503109
1000 genomesrs727503109
hgdprs727503109
ensemblrs727503109
gopubmedrs727503109
geneviewrs727503109
scholarrs727503109
googlers727503109
pharmgkbrs727503109
gwascentralrs727503109
openSNPrs727503109
23andMers727503109
23andMe allrs727503109
SNP Nexus

SNPshotrs727503109
SNPdbers727503109
MSV3drs727503109
GWAS Ctlgrs727503109
Max Magnitude0
ClinVar
Risk rs727503109(G;G)
Alt rs727503109(G;G)
Reference rs727503109(A;A)
Significance Probable-Pathogenic
Disease Rasopathy
Variation info
Gene KRAS
CLNDBN Rasopathy
Reversed 1
HGVS NC_000012.11:g.25398211T>C
CLNSRC
CLNACC RCV000150891.1,