Have questions? Visit https://www.reddit.com/r/SNPedia

rs193921065

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs193921065(C;G)
Make rs193921065(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position49619062
GeneLOC107984999, SPOP
is asnp
is mentioned by
dbSNPrs193921065
dbSNP (classic)rs193921065
ClinGenrs193921065
ebirs193921065
HLIrs193921065
Exacrs193921065
Gnomadrs193921065
Varsomers193921065
LitVarrs193921065
Maprs193921065
PheGenIrs193921065
Biobankrs193921065
1000 genomesrs193921065
hgdprs193921065
ensemblrs193921065
geneviewrs193921065
scholarrs193921065
googlers193921065
pharmgkbrs193921065
gwascentralrs193921065
openSNPrs193921065
23andMers193921065
23andMe allrs193921065
SNPshotrs193921065
SNPdbers193921065
MSV3drs193921065
GWAS Ctlgrs193921065
Max Magnitude0
ClinVar
Risk rs193921065(G;G)
Alt rs193921065(G;G)
Reference Rs193921065(C;C)
Significance Probable-Pathogenic
Disease Malignant tumor of prostate Adenocarcinoma of prostate
Variation info
Gene SPOP
CLNDBN Malignant tumor of prostate Adenocarcinoma of prostate
Reversed 1
HGVS NC_000017.10:g.47696424G>C
CLNSRC
CLNACC RCV000149021.1, RCV000435302.1,