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rs1057519967

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519967(G;G)
Make rs1057519967(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position49619063
GeneLOC107984999, SPOP
is asnp
is mentioned by
dbSNPrs1057519967
dbSNP (old)rs1057519967
ClinGenrs1057519967
ebirs1057519967
HLIrs1057519967
Exacrs1057519967
Gnomadrs1057519967
Varsomers1057519967
Maprs1057519967
PheGenIrs1057519967
Biobankrs1057519967
1000 genomesrs1057519967
hgdprs1057519967
ensemblrs1057519967
gopubmedrs1057519967
geneviewrs1057519967
scholarrs1057519967
googlers1057519967
pharmgkbrs1057519967
gwascentralrs1057519967
openSNPrs1057519967
23andMers1057519967
23andMe allrs1057519967
SNPshotrs1057519967
SNPdbers1057519967
MSV3drs1057519967
GWAS Ctlgrs1057519967
Max Magnitude0
ClinVar
Risk rs1057519967(C;C) rs1057519967(G;G)
Alt rs1057519967(C;C) rs1057519967(G;G)
Reference Rs1057519967(T;T)
Significance Probable-Pathogenic
Disease Adenocarcinoma of prostate
Variation info
Gene SPOP
CLNDBN Adenocarcinoma of prostate
Reversed 1
HGVS NC_000017.10:g.47696425A>C; NC_000017.10:g.47696425A>G
CLNSRC
CLNACC RCV000430495.1, RCV000437714.1,