rs714816
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs714816(C;C) |
Make rs714816(C;T) |
Make rs714816(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 10 |
Position | 122496829 |
Gene | HTRA1 |
is a | snp |
is | mentioned by |
dbSNP | rs714816 |
dbSNP (classic) | rs714816 |
ClinGen | rs714816 |
ebi | rs714816 |
HLI | rs714816 |
Exac | rs714816 |
Gnomad | rs714816 |
Varsome | rs714816 |
LitVar | rs714816 |
Map | rs714816 |
PheGenI | rs714816 |
Biobank | rs714816 |
1000 genomes | rs714816 |
hgdp | rs714816 |
ensembl | rs714816 |
geneview | rs714816 |
scholar | rs714816 |
rs714816 | |
pharmgkb | rs714816 |
gwascentral | rs714816 |
openSNP | rs714816 |
23andMe | rs714816 |
SNPshot | rs714816 |
SNPdbe | rs714816 |
MSV3d | rs714816 |
GWAS Ctlg | rs714816 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 27416785] Analysis of copy number variation at DMBT1 and age-related macular degeneration.