rs1071630
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1071630(C;C) |
Make rs1071630(C;T) |
Make rs1071630(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 6 |
Position | 32641349 |
Gene | HLA-DQA1, LOC107986589 |
is a | snp |
is | mentioned by |
dbSNP | rs1071630 |
dbSNP (classic) | rs1071630 |
ClinGen | rs1071630 |
ebi | rs1071630 |
HLI | rs1071630 |
Exac | rs1071630 |
Gnomad | rs1071630 |
Varsome | rs1071630 |
LitVar | rs1071630 |
Map | rs1071630 |
PheGenI | rs1071630 |
Biobank | rs1071630 |
1000 genomes | rs1071630 |
hgdp | rs1071630 |
ensembl | rs1071630 |
geneview | rs1071630 |
scholar | rs1071630 |
rs1071630 | |
pharmgkb | rs1071630 |
gwascentral | rs1071630 |
openSNP | rs1071630 |
23andMe | rs1071630 |
SNPshot | rs1071630 |
SNPdbe | rs1071630 |
MSV3d | rs1071630 |
GWAS Ctlg | rs1071630 |
Max Magnitude | 0 |
Rs1071630 is a missense variant, F41S, in HLA-DQA1.
It has been associated with Steroid-sensitive nephrotic syndrome (SSNS). [PMID 25349203]