rs1048372
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1048372(C;C) |
Make rs1048372(C;T) |
Make rs1048372(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 6 |
Position | 32642659 |
Gene | HLA-DQA1, LOC107986589 |
is a | snp |
is | mentioned by |
dbSNP | rs1048372 |
dbSNP (classic) | rs1048372 |
ClinGen | rs1048372 |
ebi | rs1048372 |
HLI | rs1048372 |
Exac | rs1048372 |
Gnomad | rs1048372 |
Varsome | rs1048372 |
LitVar | rs1048372 |
Map | rs1048372 |
PheGenI | rs1048372 |
Biobank | rs1048372 |
1000 genomes | rs1048372 |
hgdp | rs1048372 |
ensembl | rs1048372 |
geneview | rs1048372 |
scholar | rs1048372 |
rs1048372 | |
pharmgkb | rs1048372 |
gwascentral | rs1048372 |
openSNP | rs1048372 |
23andMe | rs1048372 |
SNPshot | rs1048372 |
SNPdbe | rs1048372 |
MSV3d | rs1048372 |
GWAS Ctlg | rs1048372 |
Max Magnitude | 0 |
[PMID 28717659] Identification and characterization of variants and a novel 4 bp deletion in the regulatory region of SIX6, a risk factor for primary open-angle glaucoma.