rs121913496

Orientation

minus

Stabilized

minus

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

Make rs121913496(C;C)

Make rs121913496(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

533873

Gene	HRAS, LRRC56

is a	snp
is	mentioned by
dbSNP	rs121913496
dbSNP (classic)	rs121913496
ClinGen	rs121913496
ebi	rs121913496
HLI	rs121913496
Exac	rs121913496
Gnomad	rs121913496
Varsome	rs121913496
LitVar	rs121913496
Map	rs121913496
PheGenI	rs121913496
Biobank	rs121913496
1000 genomes	rs121913496
hgdp	rs121913496
ensembl	rs121913496
geneview	rs121913496
scholar	rs121913496
google	rs121913496
pharmgkb	rs121913496
gwascentral	rs121913496
openSNP	rs121913496
23andMe	rs121913496
SNPshot	rs121913496
SNPdbe	rs121913496
MSV3d	rs121913496
GWAS Ctlg	rs121913496

Max Magnitude

0

ClinVar
Risk	rs121913496(C;C) rs121913496(T;T)
Alt	rs121913496(C;C) rs121913496(T;T)
Reference	Rs121913496(G;G)
Significance	Probable-Pathogenic
Disease	Neoplasm Transitional cell carcinoma of the bladder Neoplasm of breast Malignant melanoma of skin Squamous cell carcinoma of the head and neck Adenocarcinoma of prostate Neoplasm of the thyroid gland Adenocarcinoma of lung Squamous cell carcinoma of lung Squamous cell carcinoma of the skin
Variation	info
Gene	HRAS
CLNDBN	Neoplasm Transitional cell carcinoma of the bladder Neoplasm of breast Malignant melanoma of skin Squamous cell carcinoma of the head and neck Adenocarcinoma of prostate Neoplasm of the thyroid gland Adenocarcinoma of lung Squamous cell carcinoma of lung Squamous cell carcinoma of the skin
Reversed	1
HGVS	NC_000011.9:g.533873C>A; NC_000011.9:g.533873C>G
CLNSRC
CLNACC	RCV000420806.1, RCV000421964.1, RCV000423449.1, RCV000424686.1, RCV000433099.1, RCV000433734.1, RCV000434965.1, RCV000440259.1, RCV000442468.1, RCV000444731.1, RCV000428014.1,