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rs8102476

From SNPedia

Orientationplus
Stabilizedplus
Make rs8102476(C;C)
Make rs8102476(C;T)
Make rs8102476(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position38244973
is asnp
is mentioned by
dbSNPrs8102476
ebirs8102476
HLIrs8102476
Exacrs8102476
Varsomers8102476
Maprs8102476
PheGenIrs8102476
hapmaprs8102476
1000 genomesrs8102476
hgdprs8102476
ensemblrs8102476
gopubmedrs8102476
geneviewrs8102476
scholarrs8102476
googlers8102476
pharmgkbrs8102476
gwascentralrs8102476
openSNPrs8102476
23andMers8102476
23andMe allrs8102476
SNP Nexus

SNPshotrs8102476
SNPdbers8102476
MSV3drs8102476
GWAS Ctlgrs8102476
GMAF0.4591
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 19767754OA-icon.png] Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility
OMIM176807
Desc
Variant
Relatedalso


GET Evidence
rs8102476
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.398438
summary



[PMID 23573233OA-icon.png] Characterization of SNPs Associated with Prostate Cancer in Men of Ashkenazic Descent from the Set of GWAS Identified SNPs: Impact of Cancer Family History and Cumulative SNP Risk Prediction