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rs703556

From SNPedia

Orientationminus
Make rs703556(C;C)
Make rs703556(C;T)
Make rs703556(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position102618116
is asnp
is mentioned by
dbSNPrs703556
ebirs703556
HLIrs703556
Exacrs703556
Varsomers703556
Maprs703556
PheGenIrs703556
hapmaprs703556
1000 genomesrs703556
hgdprs703556
ensemblrs703556
gopubmedrs703556
geneviewrs703556
scholarrs703556
googlers703556
pharmgkbrs703556
gwascentralrs703556
openSNPrs703556
23andMers703556
23andMe allrs703556
SNP Nexus

SNPshotrs703556
SNPdbers703556
MSV3drs703556
GWAS Ctlgrs703556
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 26275715] A comprehensive evaluation of interaction between genetic variants and use of menopausal hormone therapy on mammographic density