rs1057519956

Orientation

plus

Stabilized

plus

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

Make rs1057519956(C;C)

Make rs1057519956(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

218583025

Gene

CNOT9

is a	snp
is	mentioned by
dbSNP	rs1057519956
dbSNP (classic)	rs1057519956
ClinGen	rs1057519956
ebi	rs1057519956
HLI	rs1057519956
Exac	rs1057519956
Gnomad	rs1057519956
Varsome	rs1057519956
LitVar	rs1057519956
Map	rs1057519956
PheGenI	rs1057519956
Biobank	rs1057519956
1000 genomes	rs1057519956
hgdp	rs1057519956
ensembl	rs1057519956
geneview	rs1057519956
scholar	rs1057519956
google	rs1057519956
pharmgkb	rs1057519956
gwascentral	rs1057519956
openSNP	rs1057519956
23andMe	rs1057519956
SNPshot	rs1057519956
SNPdbe	rs1057519956
MSV3d	rs1057519956
GWAS Ctlg	rs1057519956

Max Magnitude

0

ClinVar
Risk	rs1057519956(C;C)
Alt	rs1057519956(C;C)
Reference	Rs1057519956(T;T)
Significance	Probable-Pathogenic
Disease	Transitional cell carcinoma of the bladder Adenocarcinoma of stomach Malignant melanoma of skin Hepatocellular carcinoma Adenocarcinoma of prostate
Variation	info
Gene	RQCD1 CNOT9
CLNDBN	Transitional cell carcinoma of the bladder Adenocarcinoma of stomach Malignant melanoma of skin Hepatocellular carcinoma Adenocarcinoma of prostate
Reversed	0
HGVS	NC_000002.11:g.219447748T>C
CLNSRC
CLNACC	RCV000421602.1, RCV000422236.1, RCV000431636.1, RCV000431838.1, RCV000438382.1,