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rs1042638

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs1042638(C;T)
Make rs1042638(T;T)
ReferenceGRCh38 38.1/142
Chromosome8
Position80037711
GeneTPD52
is asnp
is mentioned by
dbSNPrs1042638
ebirs1042638
HLIrs1042638
Exacrs1042638
Varsomers1042638
Maprs1042638
PheGenIrs1042638
hapmaprs1042638
1000 genomesrs1042638
hgdprs1042638
ensemblrs1042638
gopubmedrs1042638
geneviewrs1042638
scholarrs1042638
googlers1042638
pharmgkbrs1042638
gwascentralrs1042638
openSNPrs1042638
23andMers1042638
23andMe allrs1042638
SNP Nexus

SNPshotrs1042638
SNPdbers1042638
MSV3drs1042638
GWAS Ctlgrs1042638
Max Magnitude0
A valine to leucine V660L SNP at rs1042638 appears to be associated with a moderately increased risk of breast cancer. [PMID 16614108]