rs1057519951

Orientation

minus

Stabilized

minus

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

Make rs1057519951(C;C)

Make rs1057519951(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

3

Position

49375472

Gene

RHOA

is a	snp
is	mentioned by
dbSNP	rs1057519951
dbSNP (classic)	rs1057519951
ClinGen	rs1057519951
ebi	rs1057519951
HLI	rs1057519951
Exac	rs1057519951
Gnomad	rs1057519951
Varsome	rs1057519951
LitVar	rs1057519951
Map	rs1057519951
PheGenI	rs1057519951
Biobank	rs1057519951
1000 genomes	rs1057519951
hgdp	rs1057519951
ensembl	rs1057519951
geneview	rs1057519951
scholar	rs1057519951
google	rs1057519951
pharmgkb	rs1057519951
gwascentral	rs1057519951
openSNP	rs1057519951
23andMe	rs1057519951
SNPshot	rs1057519951
SNPdbe	rs1057519951
MSV3d	rs1057519951
GWAS Ctlg	rs1057519951

Max Magnitude

0

ClinVar
Risk	rs1057519951(A;A) rs1057519951(C;C)
Alt	rs1057519951(A;A) rs1057519951(C;C)
Reference	Rs1057519951(G;G)
Significance	Probable-Pathogenic
Disease	Neoplasm of breast Adenocarcinoma of lung Adenocarcinoma of stomach Squamous cell carcinoma of the head and neck
Variation	info
Gene	RHOA
CLNDBN	Neoplasm of breast Adenocarcinoma of lung Adenocarcinoma of stomach Squamous cell carcinoma of the head and neck
Reversed	1
HGVS	NC_000003.11:g.49412905C>G; NC_000003.11:g.49412905C>T
CLNSRC
CLNACC	RCV000425677.1, RCV000425897.1, RCV000436482.1, RCV000443212.1, RCV000418248.1, RCV000428054.1, RCV000435238.1, RCV000435482.1,