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rs1057519957

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519957(C;G)
Make rs1057519957(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position218583026
GeneCNOT9
is asnp
is mentioned by
dbSNPrs1057519957
dbSNP (old)rs1057519957
ClinGenrs1057519957
ebirs1057519957
HLIrs1057519957
Exacrs1057519957
Gnomadrs1057519957
Varsomers1057519957
Maprs1057519957
PheGenIrs1057519957
Biobankrs1057519957
1000 genomesrs1057519957
hgdprs1057519957
ensemblrs1057519957
gopubmedrs1057519957
geneviewrs1057519957
scholarrs1057519957
googlers1057519957
pharmgkbrs1057519957
gwascentralrs1057519957
openSNPrs1057519957
23andMers1057519957
23andMe allrs1057519957
SNPshotrs1057519957
SNPdbers1057519957
MSV3drs1057519957
GWAS Ctlgrs1057519957
Max Magnitude0
ClinVar
Risk rs1057519957(G;G)
Alt rs1057519957(G;G)
Reference Rs1057519957(C;C)
Significance Probable-Pathogenic
Disease Transitional cell carcinoma of the bladder Adenocarcinoma of prostate Adenocarcinoma of stomach Malignant melanoma of skin Hepatocellular carcinoma
Variation info
Gene RQCD1 CNOT9
CLNDBN Transitional cell carcinoma of the bladder Adenocarcinoma of prostate Adenocarcinoma of stomach Malignant melanoma of skin Hepatocellular carcinoma
Reversed 0
HGVS NC_000002.11:g.219447749C>G
CLNSRC
CLNACC RCV000426322.1, RCV000427048.1, RCV000434591.1, RCV000443624.1, RCV000444398.1,