rs767489236
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(CAGCGGTGATAAGGCCAA;CAGCGGTGATAAGGCCAA) | 0 | common in clinvar |
Make rs767489236(-;-) |
Make rs767489236(-;CAGCGGTGATAAGGCCAA) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 15 |
Position | 28022511 |
Gene | OCA2 |
is a | snp |
is | mentioned by |
dbSNP | rs767489236 |
dbSNP (classic) | rs767489236 |
ClinGen | rs767489236 |
ebi | rs767489236 |
HLI | rs767489236 |
Exac | rs767489236 |
Gnomad | rs767489236 |
Varsome | rs767489236 |
LitVar | rs767489236 |
Map | rs767489236 |
PheGenI | rs767489236 |
Biobank | rs767489236 |
1000 genomes | rs767489236 |
hgdp | rs767489236 |
ensembl | rs767489236 |
geneview | rs767489236 |
scholar | rs767489236 |
rs767489236 | |
pharmgkb | rs767489236 |
gwascentral | rs767489236 |
openSNP | rs767489236 |
23andMe | rs767489236 |
SNPshot | rs767489236 |
SNPdbe | rs767489236 |
MSV3d | rs767489236 |
GWAS Ctlg | rs767489236 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs767489236(-;-) |
Alt | rs767489236(-;-) |
Reference | Rs767489236(CAGCGGTGATAAGGCCAA;CAGCGGTGATAAGGCCAA) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | OCA2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000015.9:g.28267657_28267674del18 |
CLNSRC | |
CLNACC | RCV000413670.1, |