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rs1057519968

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519968(G;G)
Make rs1057519968(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position49619070
GeneLOC107984999, SPOP
is asnp
is mentioned by
dbSNPrs1057519968
dbSNP (old)rs1057519968
ClinGenrs1057519968
ebirs1057519968
HLIrs1057519968
Exacrs1057519968
Gnomadrs1057519968
Varsomers1057519968
LitVarrs1057519968
Maprs1057519968
PheGenIrs1057519968
Biobankrs1057519968
1000 genomesrs1057519968
hgdprs1057519968
ensemblrs1057519968
gopubmedrs1057519968
geneviewrs1057519968
scholarrs1057519968
googlers1057519968
pharmgkbrs1057519968
gwascentralrs1057519968
openSNPrs1057519968
23andMers1057519968
23andMe allrs1057519968
SNPshotrs1057519968
SNPdbers1057519968
MSV3drs1057519968
GWAS Ctlgrs1057519968
Max Magnitude0
ClinVar
Risk rs1057519968(A;A) rs1057519968(G;G)
Alt rs1057519968(A;A) rs1057519968(G;G)
Reference Rs1057519968(T;T)
Significance Probable-Pathogenic
Disease Malignant neoplasm of body of uterus Adenocarcinoma of prostate
Variation info
Gene SPOP
CLNDBN Malignant neoplasm of body of uterus Adenocarcinoma of prostate
Reversed 1
HGVS NC_000017.10:g.47696432A>C; NC_000017.10:g.47696432A>T
CLNSRC
CLNACC RCV000431201.1, RCV000440119.1, RCV000422129.1, RCV000439381.1,