rs1057519924

Orientation

minus

Stabilized

minus

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

Make rs1057519924(G;T)

Make rs1057519924(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

177234080

Gene

NFE2L2

is a	snp
is	mentioned by
dbSNP	rs1057519924
dbSNP (classic)	rs1057519924
ClinGen	rs1057519924
ebi	rs1057519924
HLI	rs1057519924
Exac	rs1057519924
Gnomad	rs1057519924
Varsome	rs1057519924
LitVar	rs1057519924
Map	rs1057519924
PheGenI	rs1057519924
Biobank	rs1057519924
1000 genomes	rs1057519924
hgdp	rs1057519924
ensembl	rs1057519924
geneview	rs1057519924
scholar	rs1057519924
google	rs1057519924
pharmgkb	rs1057519924
gwascentral	rs1057519924
openSNP	rs1057519924
23andMe	rs1057519924
SNPshot	rs1057519924
SNPdbe	rs1057519924
MSV3d	rs1057519924
GWAS Ctlg	rs1057519924

Max Magnitude

0

ClinVar
Risk	rs1057519924(T;T)
Alt	rs1057519924(T;T)
Reference	Rs1057519924(G;G)
Significance	Probable-Pathogenic
Disease	Transitional cell carcinoma of the bladder Squamous cell carcinoma of the head and neck Adenocarcinoma of lung Hepatocellular carcinoma Squamous cell carcinoma of lung Uterine cervical neoplasms
Variation	info
Gene	NFE2L2
CLNDBN	Transitional cell carcinoma of the bladder Squamous cell carcinoma of the head and neck Adenocarcinoma of lung Hepatocellular carcinoma Squamous cell carcinoma of lung Uterine cervical neoplasms
Reversed	1
HGVS	NC_000002.11:g.178098808C>A
CLNSRC
CLNACC	RCV000426287.1, RCV000427358.1, RCV000437586.1, RCV000438261.1, RCV000442131.1, RCV000445098.1,