rs104894231

Orientation

minus

Stabilized

minus

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

Make rs104894231(A;A)

Make rs104894231(A;G)

Reference

GRCh37 37.1/132

Chromosome

11

Position

533467

Gene	HRAS, LRRC56

is a	snp
is	mentioned by
dbSNP	rs104894231
dbSNP (classic)	rs104894231
ClinGen	rs104894231
ebi	rs104894231
HLI	rs104894231
Exac	rs104894231
Gnomad	rs104894231
Varsome	rs104894231
LitVar	rs104894231
Map	rs104894231
PheGenI	rs104894231
Biobank	rs104894231
1000 genomes	rs104894231
hgdp	rs104894231
ensembl	rs104894231
geneview	rs104894231
scholar	rs104894231
google	rs104894231
pharmgkb	rs104894231
gwascentral	rs104894231
openSNP	rs104894231
23andMe	rs104894231
SNPshot	rs104894231
SNPdbe	rs104894231
MSV3d	rs104894231
GWAS Ctlg	rs104894231

Max Magnitude

0

OMIM	190020
Desc
Variant	0008
Related	also

ClinVar
Risk	rs104894231(A;A) rs104894231(C;C)
Alt	rs104894231(A;A) rs104894231(C;C)
Reference	Rs104894231(G;G)
Significance	Pathogenic
Disease	Acute myeloid leukemia Uterine cervical neoplasms Colorectal Neoplasms Multiple myeloma Adenocarcinoma of lung Adenocarcinoma of stomach Costello syndrome
Variation	info
Gene	HRAS
CLNDBN	Acute myeloid leukemia Uterine cervical neoplasms Colorectal Neoplasms Multiple myeloma Adenocarcinoma of lung Adenocarcinoma of stomach Costello syndrome
Reversed	1
HGVS	NC_000011.9:g.533467C>G; NC_000011.9:g.533467C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000417704.1, RCV000418346.1, RCV000427905.1, RCV000429488.1, RCV000439018.1, RCV000439704.1, RCV000013441.17, RCV000420974.1, RCV000427320.1, RCV000432069.1, RCV000434059.1, RCV000438623.1, RCV000444836.1,