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rs12665607

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs12665607(A;A)
Make rs12665607(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position151625494
GeneLOC105378058
is asnp
is mentioned by
dbSNPrs12665607
ebirs12665607
HLIrs12665607
Exacrs12665607
Varsomers12665607
Maprs12665607
PheGenIrs12665607
hapmaprs12665607
1000 genomesrs12665607
hgdprs12665607
ensemblrs12665607
gopubmedrs12665607
geneviewrs12665607
scholarrs12665607
googlers12665607
pharmgkbrs12665607
gwascentralrs12665607
openSNPrs12665607
23andMers12665607
23andMe allrs12665607
SNP Nexus

SNPshotrs12665607
SNPdbers12665607
MSV3drs12665607
GWAS Ctlgrs12665607
Max Magnitude0
? (A;A) (A;T) (T;T) 28
[PMID 26275715OA-icon.png] A comprehensive evaluation of interaction between genetic variants and use of menopausal hormone therapy on mammographic density
ClinVar
Risk rs12665607(A;A)
Alt rs12665607(A;A)
Reference rs12665607(T;T)
Significance Unknown
Disease Estrogen resistance
Variation info
Gene LOC105378058
CLNDBN Estrogen resistance
Reversed 0
HGVS NC_000006.11:g.151946629T>A
CLNSRC
CLNACC RCV000143993.1,