rs28934587
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in complete genomics |
Make rs28934587(C;C) |
Make rs28934587(C;T) |
Reference | GRCh37 37.1/131 |
Chromosome | 11 |
Position | 66299182 |
Gene | BBS1 |
is a | snp |
is | mentioned by |
dbSNP | rs28934587 |
dbSNP (classic) | rs28934587 |
ClinGen | rs28934587 |
ebi | rs28934587 |
HLI | rs28934587 |
Exac | rs28934587 |
Gnomad | rs28934587 |
Varsome | rs28934587 |
LitVar | rs28934587 |
Map | rs28934587 |
PheGenI | rs28934587 |
Biobank | rs28934587 |
1000 genomes | rs28934587 |
hgdp | rs28934587 |
ensembl | rs28934587 |
geneview | rs28934587 |
scholar | rs28934587 |
rs28934587 | |
pharmgkb | rs28934587 |
gwascentral | rs28934587 |
openSNP | rs28934587 |
23andMe | rs28934587 |
SNPshot | rs28934587 |
SNPdbe | rs28934587 |
MSV3d | rs28934587 |
GWAS Ctlg | rs28934587 |
Status | Deleted |
Max Magnitude | 0 |
Bardet-Biedl syndrome is a genetic disease associated with a constellation of abnormalities including obesity, pigmentary retinopathy, polydactyly, renal abnormalities, learning disabilities, and hypogenitalism.