rs1057519922

Orientation

minus

Stabilized

minus

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

Make rs1057519922(C;C)

Make rs1057519922(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

177234082

Gene

NFE2L2

is a	snp
is	mentioned by
dbSNP	rs1057519922
dbSNP (classic)	rs1057519922
ClinGen	rs1057519922
ebi	rs1057519922
HLI	rs1057519922
Exac	rs1057519922
Gnomad	rs1057519922
Varsome	rs1057519922
LitVar	rs1057519922
Map	rs1057519922
PheGenI	rs1057519922
Biobank	rs1057519922
1000 genomes	rs1057519922
hgdp	rs1057519922
ensembl	rs1057519922
geneview	rs1057519922
scholar	rs1057519922
google	rs1057519922
pharmgkb	rs1057519922
gwascentral	rs1057519922
openSNP	rs1057519922
23andMe	rs1057519922
SNPshot	rs1057519922
SNPdbe	rs1057519922
MSV3d	rs1057519922
GWAS Ctlg	rs1057519922

Max Magnitude

0

ClinVar
Risk	rs1057519922(A;A) rs1057519922(C;C)
Alt	rs1057519922(A;A) rs1057519922(C;C)
Reference	Rs1057519922(G;G)
Significance	Probable-Pathogenic
Disease	Squamous cell carcinoma of lung Transitional cell carcinoma of the bladder Hepatocellular carcinoma Uterine cervical neoplasms Adenocarcinoma of lung Squamous cell carcinoma of the head and neck
Variation	info
Gene	NFE2L2
CLNDBN	Squamous cell carcinoma of lung Transitional cell carcinoma of the bladder Hepatocellular carcinoma Uterine cervical neoplasms Adenocarcinoma of lung Squamous cell carcinoma of the head and neck
Reversed	1
HGVS	NC_000002.11:g.178098810C>G; NC_000002.11:g.178098810C>T
CLNSRC
CLNACC	RCV000419695.1, RCV000420859.1, RCV000426554.1, RCV000431138.1, RCV000436786.1, RCV000437362.1, RCV000420226.1, RCV000421132.1, RCV000428731.1, RCV000431386.1, RCV000438981.1, RCV000441372.1,