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rs121434596

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs121434596(A;A)
Make rs121434596(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position114716123
GeneNRAS
is asnp
is mentioned by
dbSNPrs121434596
ebirs121434596
HLIrs121434596
Exacrs121434596
Varsomers121434596
Maprs121434596
PheGenIrs121434596
hapmaprs121434596
1000 genomesrs121434596
hgdprs121434596
ensemblrs121434596
gopubmedrs121434596
geneviewrs121434596
scholarrs121434596
googlers121434596
pharmgkbrs121434596
gwascentralrs121434596
openSNPrs121434596
23andMers121434596
23andMe allrs121434596
SNP Nexus

SNPshotrs121434596
SNPdbers121434596
MSV3drs121434596
GWAS Ctlgrs121434596
Max Magnitude0
OMIM164790
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121434596(A,C,T;A,C,T)
Alt rs121434596(A,C,T;A,C,T)
Reference rs121434596(G;G)
Significance Pathogenic
Disease Juvenile myelomonocytic leukemia Noonan syndrome 6 RAS-associated autoimmune leukoproliferative disorder not provided
Variation info
Gene NRAS
CLNDBN Juvenile myelomonocytic leukemia Noonan syndrome 6 RAS-associated autoimmune leukoproliferative disorder not provided
Reversed 1
HGVS NC_000001.10:g.115258744C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000014915.26, RCV000022690.25, RCV000144962.2, RCV000157672.1,