rs104894226

Orientation

minus

Stabilized

minus

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

Make rs104894226(A;A)

Make rs104894226(A;G)

Reference

GRCh37 37.1/132

Chromosome

11

Position

534285

Gene	HRAS, LRRC56

is a	snp
is	mentioned by
dbSNP	rs104894226
dbSNP (classic)	rs104894226
ClinGen	rs104894226
ebi	rs104894226
HLI	rs104894226
Exac	rs104894226
Gnomad	rs104894226
Varsome	rs104894226
LitVar	rs104894226
Map	rs104894226
PheGenI	rs104894226
Biobank	rs104894226
1000 genomes	rs104894226
hgdp	rs104894226
ensembl	rs104894226
geneview	rs104894226
scholar	rs104894226
google	rs104894226
pharmgkb	rs104894226
gwascentral	rs104894226
openSNP	rs104894226
23andMe	rs104894226
SNPshot	rs104894226
SNPdbe	rs104894226
MSV3d	rs104894226
GWAS Ctlg	rs104894226

Max Magnitude

0

OMIM	190020
Desc
Variant	0005
Related	also

ClinVar
Risk	rs104894226(A;A) rs104894226(C;C) rs104894226(T;T)
Alt	rs104894226(A;A) rs104894226(C;C) rs104894226(T;T)
Reference	Rs104894226(G;G)
Significance	Pathogenic
Disease	not provided Chronic lymphocytic leukemia Hepatocellular carcinoma Adenocarcinoma of lung Pancreatic adenocarcinoma Colorectal Neoplasms Multiple myeloma Acute myeloid leukemia Adenocarcinoma of stomach Squamous cell carcinoma of lung Malignant melanoma of skin Squamous cell carcinoma of the skin Squamous cell carcinoma of the head and neck Malignant neoplasm of body of uterus Transitional cell carcinoma of the bladder Thymoma Neoplasm of breast Uterine cervical neoplasms Costello syndrome
Variation	info
Gene	HRAS
CLNDBN	not provided Chronic lymphocytic leukemia Hepatocellular carcinoma Adenocarcinoma of lung Pancreatic adenocarcinoma Colorectal Neoplasms Multiple myeloma Acute myeloid leukemia Adenocarcinoma of stomach Squamous cell carcinoma of lung Malignant melanoma of skin Squamous cell carcinoma of the skin Squamous cell carcinoma of the head and neck Malignant neoplasm of body of uterus Transitional cell carcinoma of the bladder Thymoma Neoplasm of breast Uterine cervical neoplasms Costello syndrome
Reversed	1
HGVS	NC_000011.9:g.534285C>A; NC_000011.9:g.534285C>G; NC_000011.9:g.534285C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000157914.1, RCV000418565.1, RCV000418712.1, RCV000419846.1, RCV000421468.1, RCV000424767.1, RCV000426169.1, RCV000427265.1, RCV000428389.1, RCV000429433.1, RCV000432148.1, RCV000434580.1, RCV000436822.1, RCV000437080.1, RCV000439230.1, RCV000442670.1, RCV000444507.1, RCV000444587.1, RCV000421384.1, RCV000424186.1, RCV000425652.1, RCV000426316.1, RCV000433957.1, RCV000434248.1, RCV000434457.1, RCV000440965.1, RCV000442365.1, RCV000445345.1, RCV000013438.24, RCV000157913.2, RCV000439514.1,