rs12665607
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs12665607(A;A) |
Make rs12665607(A;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 6 |
Position | 151625494 |
Gene | LOC105378058 |
is a | snp |
is | mentioned by |
dbSNP | rs12665607 |
dbSNP (classic) | rs12665607 |
ClinGen | rs12665607 |
ebi | rs12665607 |
HLI | rs12665607 |
Exac | rs12665607 |
Gnomad | rs12665607 |
Varsome | rs12665607 |
LitVar | rs12665607 |
Map | rs12665607 |
PheGenI | rs12665607 |
Biobank | rs12665607 |
1000 genomes | rs12665607 |
hgdp | rs12665607 |
ensembl | rs12665607 |
geneview | rs12665607 |
scholar | rs12665607 |
rs12665607 | |
pharmgkb | rs12665607 |
gwascentral | rs12665607 |
openSNP | rs12665607 |
23andMe | rs12665607 |
SNPshot | rs12665607 |
SNPdbe | rs12665607 |
MSV3d | rs12665607 |
GWAS Ctlg | rs12665607 |
Max Magnitude | 0 |
? | (A;A) (A;T) (T;T) | 28 |
---|---|---|
|
[PMID 26275715] 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, |