rs132630265
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
(G;T) | 4 | Choroideremia |
(T;T) | 4 | risk of Choroideremia |
Reference | GRCh38 38.1/141 |
Chromosome | X |
Position | 85894227 |
Gene | CHM |
is a | snp |
is | mentioned by |
dbSNP | rs132630265 |
dbSNP (classic) | rs132630265 |
ClinGen | rs132630265 |
ebi | rs132630265 |
HLI | rs132630265 |
Exac | rs132630265 |
Gnomad | rs132630265 |
Varsome | rs132630265 |
LitVar | rs132630265 |
Map | rs132630265 |
PheGenI | rs132630265 |
Biobank | rs132630265 |
1000 genomes | rs132630265 |
hgdp | rs132630265 |
ensembl | rs132630265 |
geneview | rs132630265 |
scholar | rs132630265 |
rs132630265 | |
pharmgkb | rs132630265 |
gwascentral | rs132630265 |
openSNP | rs132630265 |
23andMe | rs132630265 |
SNPshot | rs132630265 |
SNPdbe | rs132630265 |
MSV3d | rs132630265 |
GWAS Ctlg | rs132630265 |
Max Magnitude | 4 |
ClinVar | |
---|---|
Risk | Rs132630265(T;T) |
Alt | Rs132630265(T;T) |
Reference | Rs132630265(G;G) |
Significance | Pathogenic |
Disease | Choroideremia |
Variation | info |
Gene | CHM |
CLNDBN | Choroideremia |
Reversed | 1 |
HGVS | NC_000023.10:g.85149232C>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000011900.6, |