rs773864735
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs773864735(-;-) |
Make rs773864735(-;C) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 12 |
Position | 76346452 |
Gene | BBS10 |
is a | snp |
is | mentioned by |
dbSNP | rs773864735 |
dbSNP (classic) | rs773864735 |
ClinGen | rs773864735 |
ebi | rs773864735 |
HLI | rs773864735 |
Exac | rs773864735 |
Gnomad | rs773864735 |
Varsome | rs773864735 |
LitVar | rs773864735 |
Map | rs773864735 |
PheGenI | rs773864735 |
Biobank | rs773864735 |
1000 genomes | rs773864735 |
hgdp | rs773864735 |
ensembl | rs773864735 |
geneview | rs773864735 |
scholar | rs773864735 |
rs773864735 | |
pharmgkb | rs773864735 |
gwascentral | rs773864735 |
openSNP | rs773864735 |
23andMe | rs773864735 |
SNPshot | rs773864735 |
SNPdbe | rs773864735 |
MSV3d | rs773864735 |
GWAS Ctlg | rs773864735 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs773864735(-;-) |
Alt | rs773864735(-;-) |
Reference | Rs773864735(C;C) |
Significance | Probable-Pathogenic |
Disease | Bardet-Biedl syndrome 10 |
Variation | info |
Gene | BBS10 |
CLNDBN | Bardet-Biedl syndrome 10 |
Reversed | 0 |
HGVS | NC_000012.11:g.76740232delC |
CLNSRC | |
CLNACC | RCV000412206.1, |