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rs193929331

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs193929331(A;G)
Make rs193929331(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position25245372
GeneKRAS
is asnp
is mentioned by
dbSNPrs193929331
ebirs193929331
HLIrs193929331
Exacrs193929331
Varsomers193929331
Maprs193929331
PheGenIrs193929331
hapmaprs193929331
1000 genomesrs193929331
hgdprs193929331
ensemblrs193929331
gopubmedrs193929331
geneviewrs193929331
scholarrs193929331
googlers193929331
pharmgkbrs193929331
gwascentralrs193929331
openSNPrs193929331
23andMers193929331
23andMe allrs193929331
SNP Nexus

SNPshotrs193929331
SNPdbers193929331
MSV3drs193929331
GWAS Ctlgrs193929331
Max Magnitude0
ClinVar
Risk rs193929331(G;G)
Alt rs193929331(G;G)
Reference rs193929331(A;A)
Significance Pathogenic
Disease Noonan syndrome 3 Rasopathy
Variation info
Gene KRAS
CLNDBN Noonan syndrome 3 Rasopathy
Reversed 1
HGVS NC_000012.11:g.25398306T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000013427.19, RCV000149836.1,