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rs121913254

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913254(C;G)
Make rs121913254(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position114713909
GeneNRAS
is asnp
is mentioned by
dbSNPrs121913254
ebirs121913254
HLIrs121913254
Exacrs121913254
Varsomers121913254
Maprs121913254
PheGenIrs121913254
hapmaprs121913254
1000 genomesrs121913254
hgdprs121913254
ensemblrs121913254
gopubmedrs121913254
geneviewrs121913254
scholarrs121913254
googlers121913254
pharmgkbrs121913254
gwascentralrs121913254
openSNPrs121913254
23andMers121913254
23andMe allrs121913254
SNP Nexus

SNPshotrs121913254
SNPdbers121913254
MSV3drs121913254
GWAS Ctlgrs121913254
Max Magnitude0
ClinVar
Risk rs121913254(A,G;A,G)
Alt rs121913254(A,G;A,G)
Reference rs121913254(C;C)
Significance Pathogenic
Disease Giant pigmented hairy nevus Neurocutaneous melanosis
Variation info
Gene NRAS
CLNDBN Giant pigmented hairy nevus Neurocutaneous melanosis
Reversed 1
HGVS NC_000001.10:g.115256530G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000114746.5, RCV000144964.3,