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rs869025573

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869025573(A;A)
Make rs869025573(A;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position114716090
GeneNRAS
is asnp
is mentioned by
dbSNPrs869025573
ebirs869025573
HLIrs869025573
Exacrs869025573
Varsomers869025573
Maprs869025573
PheGenIrs869025573
hapmaprs869025573
1000 genomesrs869025573
hgdprs869025573
ensemblrs869025573
gopubmedrs869025573
geneviewrs869025573
scholarrs869025573
googlers869025573
pharmgkbrs869025573
gwascentralrs869025573
openSNPrs869025573
23andMers869025573
23andMe allrs869025573
SNP Nexus

SNPshotrs869025573
SNPdbers869025573
MSV3drs869025573
GWAS Ctlgrs869025573
Max Magnitude0
ClinVar
Risk rs869025573(A;A)
Alt rs869025573(A;A)
Reference rs869025573(T;T)
Significance Pathogenic
Disease Noonan syndrome 1
Variation info
Gene NRAS
CLNDBN Noonan syndrome 1
Reversed 1
HGVS NC_000001.10:g.115258711A>T
CLNSRC
CLNACC RCV000208553.1,