rs1057519952

Orientation

minus

Stabilized

minus

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

Make rs1057519952(C;T)

Make rs1057519952(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

3

Position

49375577

Gene

RHOA

is a	snp
is	mentioned by
dbSNP	rs1057519952
dbSNP (classic)	rs1057519952
ClinGen	rs1057519952
ebi	rs1057519952
HLI	rs1057519952
Exac	rs1057519952
Gnomad	rs1057519952
Varsome	rs1057519952
LitVar	rs1057519952
Map	rs1057519952
PheGenI	rs1057519952
Biobank	rs1057519952
1000 genomes	rs1057519952
hgdp	rs1057519952
ensembl	rs1057519952
geneview	rs1057519952
scholar	rs1057519952
google	rs1057519952
pharmgkb	rs1057519952
gwascentral	rs1057519952
openSNP	rs1057519952
23andMe	rs1057519952
SNPshot	rs1057519952
SNPdbe	rs1057519952
MSV3d	rs1057519952
GWAS Ctlg	rs1057519952

Max Magnitude

0

ClinVar
Risk	rs1057519952(T;T)
Alt	rs1057519952(T;T)
Reference	Rs1057519952(C;C)
Significance	Probable-Pathogenic
Disease	Oesophageal carcinoma Malignant lymphoma Adenocarcinoma of stomach Neoplasm of breast Colorectal Neoplasms
Variation	info
Gene	RHOA
CLNDBN	Oesophageal carcinoma Malignant lymphoma, non-Hodgkin Adenocarcinoma of stomach Neoplasm of breast Colorectal Neoplasms
Reversed	1
HGVS	NC_000003.11:g.49413010G>A
CLNSRC
CLNACC	RCV000420653.1, RCV000423113.1, RCV000430318.1, RCV000430517.1, RCV000441218.1,