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rs10263639

From SNPedia

Orientationplus
Stabilizedplus
Make rs10263639(C;C)
Make rs10263639(C;T)
Make rs10263639(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position67594280
is asnp
is mentioned by
dbSNPrs10263639
ebirs10263639
HLIrs10263639
Exacrs10263639
Varsomers10263639
Maprs10263639
PheGenIrs10263639
hapmaprs10263639
1000 genomesrs10263639
hgdprs10263639
ensemblrs10263639
gopubmedrs10263639
geneviewrs10263639
scholarrs10263639
googlers10263639
pharmgkbrs10263639
gwascentralrs10263639
openSNPrs10263639
23andMers10263639
23andMe allrs10263639
SNP Nexus

SNPshotrs10263639
SNPdbers10263639
MSV3drs10263639
GWAS Ctlgrs10263639
GMAF0.1538
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 17903305OA-icon.png]
Trait Breast cancer
Title A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study
Risk Allele
P-val 0.0000030000000000000001
Odds Ratio NR NR


GET Evidence
rs10263639
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.164062
summary