rs1057519920

Orientation

minus

Stabilized

minus

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

Make rs1057519920(C;C)

Make rs1057519920(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

177234232

Gene

NFE2L2

is a	snp
is	mentioned by
dbSNP	rs1057519920
dbSNP (classic)	rs1057519920
ClinGen	rs1057519920
ebi	rs1057519920
HLI	rs1057519920
Exac	rs1057519920
Gnomad	rs1057519920
Varsome	rs1057519920
LitVar	rs1057519920
Map	rs1057519920
PheGenI	rs1057519920
Biobank	rs1057519920
1000 genomes	rs1057519920
hgdp	rs1057519920
ensembl	rs1057519920
geneview	rs1057519920
scholar	rs1057519920
google	rs1057519920
pharmgkb	rs1057519920
gwascentral	rs1057519920
openSNP	rs1057519920
23andMe	rs1057519920
SNPshot	rs1057519920
SNPdbe	rs1057519920
MSV3d	rs1057519920
GWAS Ctlg	rs1057519920

Max Magnitude

0

ClinVar
Risk	rs1057519920(A;A) rs1057519920(C;C) rs1057519920(T;T)
Alt	rs1057519920(A;A) rs1057519920(C;C) rs1057519920(T;T)
Reference	Rs1057519920(G;G)
Significance	Probable-Pathogenic
Disease	Uterine cervical neoplasms Squamous cell carcinoma of the head and neck Transitional cell carcinoma of the bladder Renal cell carcinoma Adenocarcinoma of lung Malignant neoplasm of body of uterus Squamous cell carcinoma of lung
Variation	info
Gene	NFE2L2
CLNDBN	Uterine cervical neoplasms Squamous cell carcinoma of the head and neck Transitional cell carcinoma of the bladder Renal cell carcinoma Adenocarcinoma of lung Malignant neoplasm of body of uterus Squamous cell carcinoma of lung
Reversed	1
HGVS	NC_000002.11:g.178098960C>A; NC_000002.11:g.178098960C>G; NC_000002.11:g.178098960C>T
CLNSRC
CLNACC	RCV000418369.1, RCV000419012.1, RCV000424664.1, RCV000425738.1, RCV000430352.1, RCV000434952.1, RCV000436001.1, RCV000424276.1, RCV000427125.1, RCV000432126.1, RCV000434556.1, RCV000442314.1, RCV000442352.1, RCV000445333.1, RCV000419375.1, RCV000423965.1, RCV000429636.1, RCV000434234.1, RCV000440548.1, RCV000441021.1, RCV000441645.1,