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rs1057519958

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519958(C;T)
Make rs1057519958(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position134436505
GeneRXRA
is asnp
is mentioned by
dbSNPrs1057519958
dbSNP (old)rs1057519958
ClinGenrs1057519958
ebirs1057519958
HLIrs1057519958
Exacrs1057519958
Gnomadrs1057519958
Varsomers1057519958
Maprs1057519958
PheGenIrs1057519958
Biobankrs1057519958
1000 genomesrs1057519958
hgdprs1057519958
ensemblrs1057519958
gopubmedrs1057519958
geneviewrs1057519958
scholarrs1057519958
googlers1057519958
pharmgkbrs1057519958
gwascentralrs1057519958
openSNPrs1057519958
23andMers1057519958
23andMe allrs1057519958
SNPshotrs1057519958
SNPdbers1057519958
MSV3drs1057519958
GWAS Ctlgrs1057519958
Max Magnitude0
ClinVar
Risk rs1057519958(A;A) rs1057519958(T;T)
Alt rs1057519958(A;A) rs1057519958(T;T)
Reference Rs1057519958(C;C)
Significance Probable-Pathogenic
Disease Pancreatic adenocarcinoma Transitional cell carcinoma of the bladder Hepatocellular carcinoma
Variation info
Gene RXRA
CLNDBN Pancreatic adenocarcinoma Transitional cell carcinoma of the bladder Hepatocellular carcinoma
Reversed 0
HGVS NC_000009.11:g.137328351C>A; NC_000009.11:g.137328351C>T
CLNSRC
CLNACC RCV000419019.1, RCV000429414.1, RCV000435929.1, RCV000419754.1, RCV000425675.1, RCV000437431.1,