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rs121913237

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913237(A;A)
Make rs121913237(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position114716126
GeneNRAS
is asnp
is mentioned by
dbSNPrs121913237
ebirs121913237
HLIrs121913237
Exacrs121913237
Varsomers121913237
Maprs121913237
PheGenIrs121913237
hapmaprs121913237
1000 genomesrs121913237
hgdprs121913237
ensemblrs121913237
gopubmedrs121913237
geneviewrs121913237
scholarrs121913237
googlers121913237
pharmgkbrs121913237
gwascentralrs121913237
openSNPrs121913237
23andMers121913237
23andMe allrs121913237
SNP Nexus

SNPshotrs121913237
SNPdbers121913237
MSV3drs121913237
GWAS Ctlgrs121913237
Max Magnitude0
ClinVar
Risk rs121913237(A,C,T;A,C,T)
Alt rs121913237(A,C,T;A,C,T)
Reference rs121913237(G;G)
Significance Pathogenic
Disease Noonan syndrome not provided Myelodysplastic syndrome progressed to acute myeloid leukemia Epidermal nevus Juvenile myelomonocytic leukemia Rasopathy
Variation info
Gene NRAS
CLNDBN Noonan syndrome not provided Myelodysplastic syndrome progressed to acute myeloid leukemia Epidermal nevus Juvenile myelomonocytic leukemia Rasopathy
Reversed 1
HGVS NC_000001.10:g.115258747C>A; NC_000001.10:g.115258747C>G; NC_000001.10:g.115258747C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000037576.2, RCV000158986.1, RCV000203450.1, RCV000032849.7, RCV000144963.3, RCV000158980.1,