rs869025209
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(AAAAATGCCA;AAAAATGCCA) | 0 | common in clinvar |
Make rs869025209(-;-) |
Make rs869025209(-;AAAAATGCCA) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 12 |
Position | 76346120 |
Gene | BBS10 |
is a | snp |
is | mentioned by |
dbSNP | rs869025209 |
dbSNP (classic) | rs869025209 |
ClinGen | rs869025209 |
ebi | rs869025209 |
HLI | rs869025209 |
Exac | rs869025209 |
Gnomad | rs869025209 |
Varsome | rs869025209 |
LitVar | rs869025209 |
Map | rs869025209 |
PheGenI | rs869025209 |
Biobank | rs869025209 |
1000 genomes | rs869025209 |
hgdp | rs869025209 |
ensembl | rs869025209 |
geneview | rs869025209 |
scholar | rs869025209 |
rs869025209 | |
pharmgkb | rs869025209 |
gwascentral | rs869025209 |
openSNP | rs869025209 |
23andMe | rs869025209 |
SNPshot | rs869025209 |
SNPdbe | rs869025209 |
MSV3d | rs869025209 |
GWAS Ctlg | rs869025209 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs869025209(-;-) |
Alt | rs869025209(-;-) |
Reference | Rs869025209(AAAAATGCCA;AAAAATGCCA) |
Significance | Pathogenic |
Disease | Bardet-Biedl syndrome 10 |
Variation | info |
Gene | BBS10 |
CLNDBN | Bardet-Biedl syndrome 10 |
Reversed | 1 |
HGVS | NC_000012.11:g.76739900_76739909delTGGCATTTTT |
CLNSRC | |
CLNACC | RCV000207911.1, |