rs62636267
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs62636267(C;C) |
Make rs62636267(C;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 1 |
Position | 197427547 |
Gene | CRB1 |
is a | snp |
is | mentioned by |
dbSNP | rs62636267 |
dbSNP (classic) | rs62636267 |
ClinGen | rs62636267 |
ebi | rs62636267 |
HLI | rs62636267 |
Exac | rs62636267 |
Gnomad | rs62636267 |
Varsome | rs62636267 |
LitVar | rs62636267 |
Map | rs62636267 |
PheGenI | rs62636267 |
Biobank | rs62636267 |
1000 genomes | rs62636267 |
hgdp | rs62636267 |
ensembl | rs62636267 |
geneview | rs62636267 |
scholar | rs62636267 |
rs62636267 | |
pharmgkb | rs62636267 |
gwascentral | rs62636267 |
openSNP | rs62636267 |
23andMe | rs62636267 |
SNPshot | rs62636267 |
SNPdbe | rs62636267 |
MSV3d | rs62636267 |
GWAS Ctlg | rs62636267 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs62636267(C;C) |
Alt | rs62636267(C;C) |
Reference | Rs62636267(T;T) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | CRB1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.197396677T>C |
CLNSRC | UniProtKB (protein) |
CLNACC | RCV000086314.2, |