rs121434595

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in complete genomics

Make rs121434595(C;C)

Make rs121434595(C;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

114716124

Gene

NRAS

is a	snp
is	mentioned by
dbSNP	rs121434595
dbSNP (classic)	rs121434595
ClinGen	rs121434595
ebi	rs121434595
HLI	rs121434595
Exac	rs121434595
Gnomad	rs121434595
Varsome	rs121434595
LitVar	rs121434595
Map	rs121434595
PheGenI	rs121434595
Biobank	rs121434595
1000 genomes	rs121434595
hgdp	rs121434595
ensembl	rs121434595
geneview	rs121434595
scholar	rs121434595
google	rs121434595
pharmgkb	rs121434595
gwascentral	rs121434595
openSNP	rs121434595
23andMe	rs121434595
SNPshot	rs121434595
SNPdbe	rs121434595
MSV3d	rs121434595
GWAS Ctlg	rs121434595

Max Magnitude

0

OMIM	164790
Desc
Variant	0001
Related	also

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,