rs876657711
From SNPedia
Merged into | rs797044564 |
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(TC;TC) | 0 | common in clinvar |
Make rs876657711(-;-) |
Make rs876657711(-;CT) |
Make rs876657711(CT;CT) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 11 |
Position | 77189431 |
Gene | MYO7A |
is a | snp |
is | mentioned by |
dbSNP | rs876657711 |
dbSNP (classic) | rs876657711 |
ClinGen | rs876657711 |
ebi | rs876657711 |
HLI | rs876657711 |
Exac | rs876657711 |
Gnomad | rs876657711 |
Varsome | rs876657711 |
LitVar | rs876657711 |
Map | rs876657711 |
PheGenI | rs876657711 |
Biobank | rs876657711 |
1000 genomes | rs876657711 |
hgdp | rs876657711 |
ensembl | rs876657711 |
geneview | rs876657711 |
scholar | rs876657711 |
rs876657711 | |
pharmgkb | rs876657711 |
gwascentral | rs876657711 |
openSNP | rs876657711 |
23andMe | rs876657711 |
SNPshot | rs876657711 |
SNPdbe | rs876657711 |
MSV3d | rs876657711 |
GWAS Ctlg | rs876657711 |
Status | Merged into rs797044564 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | |
Alt | |
Reference | Rs876657711(TC;TC) |
Significance | Pathogenic |
Disease | not provided Usher syndrome |
Variation | info |
Gene | MYO7A |
CLNDBN | not provided Usher syndrome, type 1 |
Reversed | 0 |
HGVS | NC_000011.9:g.76900476_76900477delCT |
CLNSRC | |
CLNACC | RCV000171464.1, RCV000222358.1, |