rs878855095
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs878855095(A;A) |
Make rs878855095(A;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 11 |
Position | 66514662 |
Gene | BBS1 |
is a | snp |
is | mentioned by |
dbSNP | rs878855095 |
dbSNP (classic) | rs878855095 |
ClinGen | rs878855095 |
ebi | rs878855095 |
HLI | rs878855095 |
Exac | rs878855095 |
Gnomad | rs878855095 |
Varsome | rs878855095 |
LitVar | rs878855095 |
Map | rs878855095 |
PheGenI | rs878855095 |
Biobank | rs878855095 |
1000 genomes | rs878855095 |
hgdp | rs878855095 |
ensembl | rs878855095 |
geneview | rs878855095 |
scholar | rs878855095 |
rs878855095 | |
pharmgkb | rs878855095 |
gwascentral | rs878855095 |
openSNP | rs878855095 |
23andMe | rs878855095 |
SNPshot | rs878855095 |
SNPdbe | rs878855095 |
MSV3d | rs878855095 |
GWAS Ctlg | rs878855095 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs878855095(A;A) |
Alt | rs878855095(A;A) |
Reference | Rs878855095(G;G) |
Significance | Pathogenic |
Disease | Bardet-Biedl syndrome |
Variation | info |
Gene | BBS1 |
CLNDBN | Bardet-Biedl syndrome |
Reversed | 0 |
HGVS | NC_000011.9:g.66282133G>A |
CLNSRC | |
CLNACC | RCV000230074.1, |