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rs121913250

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913250(G;T)
Make rs121913250(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position114716127
GeneNRAS
is asnp
is mentioned by
dbSNPrs121913250
dbSNP (classic)rs121913250
ClinGenrs121913250
ebirs121913250
HLIrs121913250
Exacrs121913250
Gnomadrs121913250
Varsomers121913250
LitVarrs121913250
Maprs121913250
PheGenIrs121913250
Biobankrs121913250
1000 genomesrs121913250
hgdprs121913250
ensemblrs121913250
geneviewrs121913250
scholarrs121913250
googlers121913250
pharmgkbrs121913250
gwascentralrs121913250
openSNPrs121913250
23andMers121913250
SNPshotrs121913250
SNPdbers121913250
MSV3drs121913250
GWAS Ctlgrs121913250
Max Magnitude0
ClinVar
Risk rs121913250(A;A) rs121913250(C;C) rs121913250(T;T)
Alt rs121913250(A;A) rs121913250(C;C) rs121913250(T;T)
Reference Rs121913250(G;G)
Significance Pathogenic
Disease not provided Malignant neoplasm of body of uterus Colorectal Neoplasms Multiple myeloma Adenocarcinoma of stomach Acute myeloid leukemia Malignant melanoma of skin Non-small cell lung cancer Malignant melanoma Myelodysplastic syndrome Chronic myeloid leukemia Rasopathy
Variation info
Gene NRAS
CLNDBN not provided Malignant neoplasm of body of uterus Colorectal Neoplasms Multiple myeloma Adenocarcinoma of stomach Acute myeloid leukemia Malignant melanoma of skin Non-small cell lung cancer Malignant melanoma Myelodysplastic syndrome Chronic myeloid leukemia Rasopathy
Reversed 1
HGVS NC_000001.10:g.115258748C>A; NC_000001.10:g.115258748C>G; NC_000001.10:g.115258748C>T
CLNSRC UniProtKB (protein)
CLNACC RCV000158979.1, RCV000422059.1, RCV000422738.1, RCV000425805.1, RCV000432311.1, RCV000433830.1, RCV000435186.1, RCV000440380.1, RCV000444830.1, RCV000445013.1, RCV000158985.2, RCV000420396.1, RCV000420637.1, RCV000423088.1, RCV000425150.1, RCV000430032.1, RCV000430635.1, RCV000435447.1, RCV000438291.1, RCV000440262.1, RCV000444217.1, RCV000158978.2, RCV000212761.1, RCV000421327.1, RCV000421993.1, RCV000427184.1, RCV000430288.1, RCV000431995.1, RCV000433097.1, RCV000439216.1, RCV000442594.1, RCV000445150.1,