rs1057519953

Orientation

minus

Stabilized

minus

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

Make rs1057519953(A;A)

Make rs1057519953(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

3

Position

49375576

Gene

RHOA

is a	snp
is	mentioned by
dbSNP	rs1057519953
dbSNP (classic)	rs1057519953
ClinGen	rs1057519953
ebi	rs1057519953
HLI	rs1057519953
Exac	rs1057519953
Gnomad	rs1057519953
Varsome	rs1057519953
LitVar	rs1057519953
Map	rs1057519953
PheGenI	rs1057519953
Biobank	rs1057519953
1000 genomes	rs1057519953
hgdp	rs1057519953
ensembl	rs1057519953
geneview	rs1057519953
scholar	rs1057519953
google	rs1057519953
pharmgkb	rs1057519953
gwascentral	rs1057519953
openSNP	rs1057519953
23andMe	rs1057519953
SNPshot	rs1057519953
SNPdbe	rs1057519953
MSV3d	rs1057519953
GWAS Ctlg	rs1057519953

Max Magnitude

0

ClinVar
Risk	rs1057519953(A;A) rs1057519953(T;T)
Alt	rs1057519953(A;A) rs1057519953(T;T)
Reference	Rs1057519953(G;G)
Significance	Probable-Pathogenic
Disease	Malignant lymphoma Oesophageal carcinoma Colorectal Neoplasms Adenocarcinoma of stomach Neoplasm of breast
Variation	info
Gene	RHOA
CLNDBN	Malignant lymphoma, non-Hodgkin Oesophageal carcinoma Colorectal Neoplasms Adenocarcinoma of stomach Neoplasm of breast
Reversed	1
HGVS	NC_000003.11:g.49413009C>A; NC_000003.11:g.49413009C>T
CLNSRC
CLNACC	RCV000425080.1, RCV000431457.1, RCV000432532.1, RCV000443944.1, RCV000444013.1, RCV000421840.1, RCV000422905.1, RCV000432727.1, RCV000440078.1, RCV000444856.1,