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rs1057519921

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057519921(A;G)
Make rs1057519921(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position177234231
GeneNFE2L2
is asnp
is mentioned by
dbSNPrs1057519921
dbSNP (old)rs1057519921
ClinGenrs1057519921
ebirs1057519921
HLIrs1057519921
Exacrs1057519921
Gnomadrs1057519921
Varsomers1057519921
Maprs1057519921
PheGenIrs1057519921
Biobankrs1057519921
1000 genomesrs1057519921
hgdprs1057519921
ensemblrs1057519921
gopubmedrs1057519921
geneviewrs1057519921
scholarrs1057519921
googlers1057519921
pharmgkbrs1057519921
gwascentralrs1057519921
openSNPrs1057519921
23andMers1057519921
23andMe allrs1057519921
SNPshotrs1057519921
SNPdbers1057519921
MSV3drs1057519921
GWAS Ctlgrs1057519921
Max Magnitude0
ClinVar
Risk rs1057519921(G;G)
Alt rs1057519921(G;G)
Reference Rs1057519921(A;A)
Significance Probable-Pathogenic
Disease Transitional cell carcinoma of the bladder Malignant neoplasm of body of uterus Uterine cervical neoplasms Renal cell carcinoma Squamous cell carcinoma of the head and neck Adenocarcinoma of lung Squamous cell carcinoma of lung
Variation info
Gene NFE2L2
CLNDBN Transitional cell carcinoma of the bladder Malignant neoplasm of body of uterus Uterine cervical neoplasms Renal cell carcinoma Squamous cell carcinoma of the head and neck Adenocarcinoma of lung Squamous cell carcinoma of lung
Reversed 1
HGVS NC_000002.11:g.178098959T>C
CLNSRC
CLNACC RCV000421608.1, RCV000425359.1, RCV000426059.1, RCV000431763.1, RCV000432841.1, RCV000441859.1, RCV000441968.1,