rs1057519923

Orientation

minus

Stabilized

minus

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

Make rs1057519923(A;T)

Make rs1057519923(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

177234081

Gene

NFE2L2

is a	snp
is	mentioned by
dbSNP	rs1057519923
dbSNP (classic)	rs1057519923
ClinGen	rs1057519923
ebi	rs1057519923
HLI	rs1057519923
Exac	rs1057519923
Gnomad	rs1057519923
Varsome	rs1057519923
LitVar	rs1057519923
Map	rs1057519923
PheGenI	rs1057519923
Biobank	rs1057519923
1000 genomes	rs1057519923
hgdp	rs1057519923
ensembl	rs1057519923
geneview	rs1057519923
scholar	rs1057519923
google	rs1057519923
pharmgkb	rs1057519923
gwascentral	rs1057519923
openSNP	rs1057519923
23andMe	rs1057519923
SNPshot	rs1057519923
SNPdbe	rs1057519923
MSV3d	rs1057519923
GWAS Ctlg	rs1057519923

Max Magnitude

0

ClinVar
Risk	rs1057519923(T;T)
Alt	rs1057519923(T;T)
Reference	Rs1057519923(A;A)
Significance	Probable-Pathogenic
Disease	Uterine cervical neoplasms Squamous cell carcinoma of lung Squamous cell carcinoma of the head and neck Adenocarcinoma of lung Transitional cell carcinoma of the bladder Hepatocellular carcinoma
Variation	info
Gene	NFE2L2
CLNDBN	Uterine cervical neoplasms Squamous cell carcinoma of lung Squamous cell carcinoma of the head and neck Adenocarcinoma of lung Transitional cell carcinoma of the bladder Hepatocellular carcinoma
Reversed	1
HGVS	NC_000002.11:g.178098809T>A
CLNSRC
CLNACC	RCV000422224.1, RCV000423337.1, RCV000432493.1, RCV000433603.1, RCV000439873.1, RCV000442257.1,