rs770556842
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(AGTT;AGTT) | 0 | common in clinvar |
Make rs770556842(-;-) |
Make rs770556842(-;AGTT) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 12 |
Position | 76346383 |
Gene | BBS10 |
is a | snp |
is | mentioned by |
dbSNP | rs770556842 |
dbSNP (classic) | rs770556842 |
ClinGen | rs770556842 |
ebi | rs770556842 |
HLI | rs770556842 |
Exac | rs770556842 |
Gnomad | rs770556842 |
Varsome | rs770556842 |
LitVar | rs770556842 |
Map | rs770556842 |
PheGenI | rs770556842 |
Biobank | rs770556842 |
1000 genomes | rs770556842 |
hgdp | rs770556842 |
ensembl | rs770556842 |
geneview | rs770556842 |
scholar | rs770556842 |
rs770556842 | |
pharmgkb | rs770556842 |
gwascentral | rs770556842 |
openSNP | rs770556842 |
23andMe | rs770556842 |
SNPshot | rs770556842 |
SNPdbe | rs770556842 |
MSV3d | rs770556842 |
GWAS Ctlg | rs770556842 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs770556842(-;-) |
Alt | rs770556842(-;-) |
Reference | Rs770556842(AGTT;AGTT) |
Significance | Probable-Pathogenic |
Disease | Bardet-Biedl syndrome 10 |
Variation | info |
Gene | BBS10 |
CLNDBN | Bardet-Biedl syndrome 10 |
Reversed | 0 |
HGVS | NC_000012.11:g.76740163_76740166delAGTT |
CLNSRC | |
CLNACC | RCV000169372.1, |