rs121913233

Orientation

minus

Stabilized

minus

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

Make rs121913233(A;T)

Make rs121913233(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

533874

Gene	HRAS, LRRC56

is a	snp
is	mentioned by
dbSNP	rs121913233
dbSNP (classic)	rs121913233
ClinGen	rs121913233
ebi	rs121913233
HLI	rs121913233
Exac	rs121913233
Gnomad	rs121913233
Varsome	rs121913233
LitVar	rs121913233
Map	rs121913233
PheGenI	rs121913233
Biobank	rs121913233
1000 genomes	rs121913233
hgdp	rs121913233
ensembl	rs121913233
geneview	rs121913233
scholar	rs121913233
google	rs121913233
pharmgkb	rs121913233
gwascentral	rs121913233
openSNP	rs121913233
23andMe	rs121913233
SNPshot	rs121913233
SNPdbe	rs121913233
MSV3d	rs121913233
GWAS Ctlg	rs121913233

Max Magnitude

0

ClinVar
Risk	rs121913233(C;C) rs121913233(G;G) rs121913233(T;T)
Alt	rs121913233(C;C) rs121913233(G;G) rs121913233(T;T)
Reference	Rs121913233(A;A)
Significance	Pathogenic
Disease	Hepatocellular carcinoma Squamous cell carcinoma of the head and neck Colorectal Neoplasms Malignant neoplasm of body of uterus Malignant melanoma of skin Pancreatic adenocarcinoma Acute myeloid leukemia Adenocarcinoma of stomach Transitional cell carcinoma of the bladder Chronic lymphocytic leukemia Adenocarcinoma of lung Squamous cell carcinoma of lung Multiple myeloma Adenocarcinoma of prostate Neoplasm of breast Neoplasm of the thyroid gland Squamous cell carcinoma of the skin Epidermal nevus syndrome not specified Neoplasm
Variation	info
Gene	HRAS
CLNDBN	Hepatocellular carcinoma Squamous cell carcinoma of the head and neck Colorectal Neoplasms Malignant neoplasm of body of uterus Malignant melanoma of skin Pancreatic adenocarcinoma Acute myeloid leukemia Adenocarcinoma of stomach Transitional cell carcinoma of the bladder Chronic lymphocytic leukemia Adenocarcinoma of lung Squamous cell carcinoma of lung Multiple myeloma Adenocarcinoma of prostate Neoplasm of breast Neoplasm of the thyroid gland Squamous cell carcinoma of the skin Epidermal nevus syndrome not specified Neoplasm
Reversed	1
HGVS	NC_000011.9:g.533874T>A; NC_000011.9:g.533874T>C; NC_000011.9:g.533874T>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000420395.1, RCV000420623.1, RCV000421690.1, RCV000421974.1, RCV000425694.1, RCV000426826.1, RCV000428206.1, RCV000428443.1, RCV000430634.1, RCV000433098.1, RCV000436845.1, RCV000437079.1, RCV000438263.1, RCV000438465.1, RCV000439626.1, RCV000445166.1, RCV000445204.1, RCV000148033.4, RCV000157918.1, RCV000418550.1, RCV000437086.1, RCV000417619.1, RCV000419094.1, RCV000420448.1, RCV000424105.1, RCV000425877.1, RCV000428681.1, RCV000428741.1, RCV000430030.1, RCV000430658.1, RCV000435275.1, RCV000435489.1, RCV000435915.1, RCV000440764.1, RCV000441832.1,