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rs121434595

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs121434595(C;C)
Make rs121434595(C;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position114716124
GeneNRAS
is asnp
is mentioned by
dbSNPrs121434595
dbSNP (classic)rs121434595
ClinGenrs121434595
ebirs121434595
HLIrs121434595
Exacrs121434595
Gnomadrs121434595
Varsomers121434595
LitVarrs121434595
Maprs121434595
PheGenIrs121434595
Biobankrs121434595
1000 genomesrs121434595
hgdprs121434595
ensemblrs121434595
geneviewrs121434595
scholarrs121434595
googlers121434595
pharmgkbrs121434595
gwascentralrs121434595
openSNPrs121434595
23andMers121434595
SNPshotrs121434595
SNPdbers121434595
MSV3drs121434595
GWAS Ctlgrs121434595
Max Magnitude0
OMIM164790
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121434595(A;A) rs121434595(C;C) rs121434595(T;T)
Alt rs121434595(A;A) rs121434595(C;C) rs121434595(T;T)
Reference Rs121434595(G;G)
Significance Pathogenic
Disease Malignant melanoma Carcinoma of colon Giant pigmented hairy nevus Medulloblastoma Transitional cell carcinoma of the bladder Multiple myeloma Adenocarcinoma of stomach Myelodysplastic syndrome Colorectal Neoplasms Malignant lymphoma Acute myeloid leukemia Malignant melanoma of skin Neoplasm of stomach
Variation info
Gene NRAS
CLNDBN Malignant melanoma Carcinoma of colon Giant pigmented hairy nevus Medulloblastoma Transitional cell carcinoma of the bladder Multiple myeloma Adenocarcinoma of stomach Myelodysplastic syndrome Colorectal Neoplasms Malignant lymphoma, non-Hodgkin Acute myeloid leukemia Malignant melanoma of skin Neoplasm of stomach
Reversed 1
HGVS NC_000001.10:g.115258745C>A; NC_000001.10:g.115258745C>G; NC_000001.10:g.115258745C>T
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000445167.1, RCV000014913.5, RCV000114743.4, RCV000419545.1, RCV000419583.1, RCV000424942.1, RCV000426328.1, RCV000427817.1, RCV000428963.1, RCV000434327.1, RCV000437450.1, RCV000438070.1, RCV000444449.1, RCV000436341.1,