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rs121913250

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913250(G;T)
Make rs121913250(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position114716127
GeneNRAS
is asnp
is mentioned by
dbSNPrs121913250
ebirs121913250
HLIrs121913250
Exacrs121913250
Varsomers121913250
Maprs121913250
PheGenIrs121913250
hapmaprs121913250
1000 genomesrs121913250
hgdprs121913250
ensemblrs121913250
gopubmedrs121913250
geneviewrs121913250
scholarrs121913250
googlers121913250
pharmgkbrs121913250
gwascentralrs121913250
openSNPrs121913250
23andMers121913250
23andMe allrs121913250
SNP Nexus

SNPshotrs121913250
SNPdbers121913250
MSV3drs121913250
GWAS Ctlgrs121913250
Max Magnitude0
ClinVar
Risk rs121913250(A,C,T;A,C,T)
Alt rs121913250(A,C,T;A,C,T)
Reference rs121913250(G;G)
Significance Pathogenic
Disease not provided Rasopathy
Variation info
Gene NRAS
CLNDBN not provided Rasopathy
Reversed 1
HGVS NC_000001.10:g.115258748C>A; NC_000001.10:g.115258748C>G; NC_000001.10:g.115258748C>T
CLNSRC
CLNACC RCV000158979.1, RCV000158985.2, RCV000158978.2, RCV000212761.1,