rs121913254

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs121913254(C;G)

Make rs121913254(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

114713909

Gene

NRAS

is a	snp
is	mentioned by
dbSNP	rs121913254
dbSNP (classic)	rs121913254
ClinGen	rs121913254
ebi	rs121913254
HLI	rs121913254
Exac	rs121913254
Gnomad	rs121913254
Varsome	rs121913254
LitVar	rs121913254
Map	rs121913254
PheGenI	rs121913254
Biobank	rs121913254
1000 genomes	rs121913254
hgdp	rs121913254
ensembl	rs121913254
geneview	rs121913254
scholar	rs121913254
google	rs121913254
pharmgkb	rs121913254
gwascentral	rs121913254
openSNP	rs121913254
23andMe	rs121913254
SNPshot	rs121913254
SNPdbe	rs121913254
MSV3d	rs121913254
GWAS Ctlg	rs121913254

Max Magnitude

0

ClinVar
Risk	rs121913254(A;A) rs121913254(G;G) rs121913254(T;T)
Alt	rs121913254(A;A) rs121913254(G;G) rs121913254(T;T)
Reference	Rs121913254(C;C)
Significance	Pathogenic
Disease	Malignant melanoma Giant pigmented hairy nevus Neurocutaneous melanosis Chronic lymphocytic leukemia Acute myeloid leukemia Renal cell carcinoma Neuroblastoma Non-small cell lung cancer Nasopharyngeal Neoplasms Glioblastoma Transitional cell carcinoma of the bladder Adrenocortical carcinoma Adenocarcinoma of lung Neoplasm of brain Malignant neoplasm of body of uterus Malignant melanoma of skin Adenocarcinoma of stomach Hepatocellular carcinoma Ovarian Serous Cystadenocarcinoma Colorectal Neoplasms Multiple myeloma
Variation	info
Gene	NRAS
CLNDBN	Malignant melanoma Giant pigmented hairy nevus Neurocutaneous melanosis Chronic lymphocytic leukemia Acute myeloid leukemia Renal cell carcinoma Neuroblastoma Non-small cell lung cancer Nasopharyngeal Neoplasms Glioblastoma Transitional cell carcinoma of the bladder Adrenocortical carcinoma Adenocarcinoma of lung Neoplasm of brain Malignant neoplasm of body of uterus Malignant melanoma of skin Adenocarcinoma of stomach Hepatocellular carcinoma Ovarian Serous Cystadenocarcinoma Colorectal Neoplasms Multiple myeloma
Reversed	1
HGVS	NC_000001.10:g.115256530G>A; NC_000001.10:g.115256530G>C; NC_000001.10:g.115256530G>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000425052.1, RCV000427189.1, RCV000114746.5, RCV000144964.3, RCV000418269.1, RCV000418907.1, RCV000423012.1, RCV000423656.1, RCV000425440.1, RCV000426976.1, RCV000428264.1, RCV000428499.1, RCV000431313.1, RCV000433274.1, RCV000434388.1, RCV000435041.1, RCV000436588.1, RCV000436806.1, RCV000441348.1, RCV000441559.1, RCV000443974.1, RCV000444538.1, RCV000444882.1,