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

rs397517042

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397517042(G;G)
Make rs397517042(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position25209896
GeneKRAS
is asnp
is mentioned by
dbSNPrs397517042
ebirs397517042
HLIrs397517042
Exacrs397517042
Varsomers397517042
Maprs397517042
PheGenIrs397517042
hapmaprs397517042
1000 genomesrs397517042
hgdprs397517042
ensemblrs397517042
gopubmedrs397517042
geneviewrs397517042
scholarrs397517042
googlers397517042
pharmgkbrs397517042
gwascentralrs397517042
openSNPrs397517042
23andMers397517042
23andMe allrs397517042
SNP Nexus

SNPshotrs397517042
SNPdbers397517042
MSV3drs397517042
GWAS Ctlgrs397517042
Max Magnitude0
ClinVar
Risk rs397517042(A,G;A,G)
Alt rs397517042(A,G;A,G)
Reference rs397517042(T;T)
Significance Pathogenic
Disease Noonan syndrome not provided Rasopathy
Variation info
Gene KRAS
CLNDBN Noonan syndrome not provided Rasopathy
Reversed 1
HGVS NC_000012.11:g.25362830A>C; NC_000012.11:g.25362830A>T
CLNSRC
CLNACC RCV000038275.3, RCV000157941.1, RCV000150884.1,