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rs1057519956

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519956(C;C)
Make rs1057519956(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position218583025
GeneCNOT9
is asnp
is mentioned by
dbSNPrs1057519956
dbSNP (old)rs1057519956
ClinGenrs1057519956
ebirs1057519956
HLIrs1057519956
Exacrs1057519956
Gnomadrs1057519956
Varsomers1057519956
Maprs1057519956
PheGenIrs1057519956
Biobankrs1057519956
1000 genomesrs1057519956
hgdprs1057519956
ensemblrs1057519956
gopubmedrs1057519956
geneviewrs1057519956
scholarrs1057519956
googlers1057519956
pharmgkbrs1057519956
gwascentralrs1057519956
openSNPrs1057519956
23andMers1057519956
23andMe allrs1057519956
SNPshotrs1057519956
SNPdbers1057519956
MSV3drs1057519956
GWAS Ctlgrs1057519956
Max Magnitude0
ClinVar
Risk rs1057519956(C;C)
Alt rs1057519956(C;C)
Reference Rs1057519956(T;T)
Significance Probable-Pathogenic
Disease Transitional cell carcinoma of the bladder Adenocarcinoma of stomach Malignant melanoma of skin Hepatocellular carcinoma Adenocarcinoma of prostate
Variation info
Gene RQCD1 CNOT9
CLNDBN Transitional cell carcinoma of the bladder Adenocarcinoma of stomach Malignant melanoma of skin Hepatocellular carcinoma Adenocarcinoma of prostate
Reversed 0
HGVS NC_000002.11:g.219447748T>C
CLNSRC
CLNACC RCV000421602.1, RCV000422236.1, RCV000431636.1, RCV000431838.1, RCV000438382.1,