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rs1057519924

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519924(G;T)
Make rs1057519924(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position177234080
GeneNFE2L2
is asnp
is mentioned by
dbSNPrs1057519924
dbSNP (classic)rs1057519924
ClinGenrs1057519924
ebirs1057519924
HLIrs1057519924
Exacrs1057519924
Gnomadrs1057519924
Varsomers1057519924
LitVarrs1057519924
Maprs1057519924
PheGenIrs1057519924
Biobankrs1057519924
1000 genomesrs1057519924
hgdprs1057519924
ensemblrs1057519924
geneviewrs1057519924
scholarrs1057519924
googlers1057519924
pharmgkbrs1057519924
gwascentralrs1057519924
openSNPrs1057519924
23andMers1057519924
23andMe allrs1057519924
SNPshotrs1057519924
SNPdbers1057519924
MSV3drs1057519924
GWAS Ctlgrs1057519924
Max Magnitude0
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,