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rs1057519923

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057519923(A;T)
Make rs1057519923(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position177234081
GeneNFE2L2
is asnp
is mentioned by
dbSNPrs1057519923
dbSNP (old)rs1057519923
ClinGenrs1057519923
ebirs1057519923
HLIrs1057519923
Exacrs1057519923
Gnomadrs1057519923
Varsomers1057519923
LitVarrs1057519923
Maprs1057519923
PheGenIrs1057519923
Biobankrs1057519923
1000 genomesrs1057519923
hgdprs1057519923
ensemblrs1057519923
gopubmedrs1057519923
geneviewrs1057519923
scholarrs1057519923
googlers1057519923
pharmgkbrs1057519923
gwascentralrs1057519923
openSNPrs1057519923
23andMers1057519923
23andMe allrs1057519923
SNPshotrs1057519923
SNPdbers1057519923
MSV3drs1057519923
GWAS Ctlgrs1057519923
Max Magnitude0
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,