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rs397517041

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397517041(G;T)
Make rs397517041(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position25209908
GeneKRAS
is asnp
is mentioned by
dbSNPrs397517041
ebirs397517041
HLIrs397517041
Exacrs397517041
Varsomers397517041
Maprs397517041
PheGenIrs397517041
hapmaprs397517041
1000 genomesrs397517041
hgdprs397517041
ensemblrs397517041
gopubmedrs397517041
geneviewrs397517041
scholarrs397517041
googlers397517041
pharmgkbrs397517041
gwascentralrs397517041
openSNPrs397517041
23andMers397517041
23andMe allrs397517041
SNP Nexus

SNPshotrs397517041
SNPdbers397517041
MSV3drs397517041
GWAS Ctlgrs397517041
Max Magnitude0
ClinVar
Risk rs397517041(T;T)
Alt rs397517041(T;T)
Reference rs397517041(G;G)
Significance Probable-Pathogenic
Disease Noonan syndrome
Variation info
Gene KRAS
CLNDBN Noonan syndrome
Reversed 1
HGVS NC_000012.11:g.25362842C>A
CLNSRC ClinVar
CLNACC RCV000038273.2,