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rs1057519966

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519966(G;G)
Make rs1057519966(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position49619064
GeneLOC107984999, SPOP
is asnp
is mentioned by
dbSNPrs1057519966
dbSNP (classic)rs1057519966
ClinGenrs1057519966
ebirs1057519966
HLIrs1057519966
Exacrs1057519966
Gnomadrs1057519966
Varsomers1057519966
LitVarrs1057519966
Maprs1057519966
PheGenIrs1057519966
Biobankrs1057519966
1000 genomesrs1057519966
hgdprs1057519966
ensemblrs1057519966
geneviewrs1057519966
scholarrs1057519966
googlers1057519966
pharmgkbrs1057519966
gwascentralrs1057519966
openSNPrs1057519966
23andMers1057519966
SNPshotrs1057519966
SNPdbers1057519966
MSV3drs1057519966
GWAS Ctlgrs1057519966
Max Magnitude0
ClinVar
Risk rs1057519966(A;A) rs1057519966(G;G)
Alt rs1057519966(A;A) rs1057519966(G;G)
Reference Rs1057519966(T;T)
Significance Probable-Pathogenic
Disease Adenocarcinoma of prostate
Variation info
Gene SPOP
CLNDBN Adenocarcinoma of prostate
Reversed 1
HGVS NC_000017.10:g.47696426A>C; NC_000017.10:g.47696426A>T
CLNSRC
CLNACC RCV000418078.1, RCV000420500.1,