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rs121913248

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913248(A;A)
Make rs121913248(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position114716109
GeneNRAS
is asnp
is mentioned by
dbSNPrs121913248
dbSNP (classic)rs121913248
ClinGenrs121913248
ebirs121913248
HLIrs121913248
Exacrs121913248
Gnomadrs121913248
Varsomers121913248
LitVarrs121913248
Maprs121913248
PheGenIrs121913248
Biobankrs121913248
1000 genomesrs121913248
hgdprs121913248
ensemblrs121913248
geneviewrs121913248
scholarrs121913248
googlers121913248
pharmgkbrs121913248
gwascentralrs121913248
openSNPrs121913248
23andMers121913248
23andMe allrs121913248
SNPshotrs121913248
SNPdbers121913248
MSV3drs121913248
GWAS Ctlgrs121913248
Max Magnitude0
ClinVar
Risk rs121913248(A;A) rs121913248(C;C)
Alt rs121913248(A;A) rs121913248(C;C)
Reference Rs121913248(G;G)
Significance Probable-Pathogenic
Disease Malignant melanoma
Variation info
Gene NRAS
CLNDBN Malignant melanoma
Reversed 1
HGVS NC_000001.10:g.115258730C>T
CLNSRC
CLNACC RCV000435339.1,