rs1120638
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1120638(A;A) |
Make rs1120638(A;G) |
Make rs1120638(G;G) |
Reference | GRCh37.p2 37.2/134 |
Chromosome | Y |
Position | 3649707 |
is a | snp |
is | mentioned by |
dbSNP | rs1120638 |
dbSNP (classic) | rs1120638 |
ClinGen | rs1120638 |
ebi | rs1120638 |
HLI | rs1120638 |
Exac | rs1120638 |
Gnomad | rs1120638 |
Varsome | rs1120638 |
LitVar | rs1120638 |
Map | rs1120638 |
PheGenI | rs1120638 |
Biobank | rs1120638 |
1000 genomes | rs1120638 |
hgdp | rs1120638 |
ensembl | rs1120638 |
geneview | rs1120638 |
scholar | rs1120638 |
rs1120638 | |
pharmgkb | rs1120638 |
gwascentral | rs1120638 |
openSNP | rs1120638 |
23andMe | rs1120638 |
SNPshot | rs1120638 |
SNPdbe | rs1120638 |
MSV3d | rs1120638 |
GWAS Ctlg | rs1120638 |
Y Chrom | rs1120638 |
Max Magnitude | 0 |
[PMID 21882634] [Influence of genetic mutations on clinical presentation of subretinal neovascularization. Report 2: The impact of HTRA and VEGF genes polymorphism][PMID 18493315] C2 and CFB genes in age-related maculopathy and joint action with CFH and LOC387715 genes.