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rs1057519922

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519922(C;C)
Make rs1057519922(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position177234082
GeneNFE2L2
is asnp
is mentioned by
dbSNPrs1057519922
dbSNP (old)rs1057519922
ClinGenrs1057519922
ebirs1057519922
HLIrs1057519922
Exacrs1057519922
Gnomadrs1057519922
Varsomers1057519922
Maprs1057519922
PheGenIrs1057519922
Biobankrs1057519922
1000 genomesrs1057519922
hgdprs1057519922
ensemblrs1057519922
gopubmedrs1057519922
geneviewrs1057519922
scholarrs1057519922
googlers1057519922
pharmgkbrs1057519922
gwascentralrs1057519922
openSNPrs1057519922
23andMers1057519922
23andMe allrs1057519922
SNPshotrs1057519922
SNPdbers1057519922
MSV3drs1057519922
GWAS Ctlgrs1057519922
Max Magnitude0
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,