rs587778875
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs587778875(-;C) |
Make rs587778875(C;C) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 2 |
Position | 38074520 |
Gene | CYP1B1 |
is a | snp |
is | mentioned by |
dbSNP | rs587778875 |
dbSNP (classic) | rs587778875 |
ClinGen | rs587778875 |
ebi | rs587778875 |
HLI | rs587778875 |
Exac | rs587778875 |
Gnomad | rs587778875 |
Varsome | rs587778875 |
LitVar | rs587778875 |
Map | rs587778875 |
PheGenI | rs587778875 |
Biobank | rs587778875 |
1000 genomes | rs587778875 |
hgdp | rs587778875 |
ensembl | rs587778875 |
geneview | rs587778875 |
scholar | rs587778875 |
rs587778875 | |
pharmgkb | rs587778875 |
gwascentral | rs587778875 |
openSNP | rs587778875 |
23andMe | rs587778875 |
SNPshot | rs587778875 |
SNPdbe | rs587778875 |
MSV3d | rs587778875 |
GWAS Ctlg | rs587778875 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587778875(C;C) |
Alt | rs587778875(C;C) |
Reference | Rs587778875(-;-) |
Significance | Pathogenic |
Disease | Coloboma not provided |
Variation | info |
Gene | CYP1B1 |
CLNDBN | Coloboma not provided |
Reversed | 1 |
HGVS | NC_000002.11:g.38301664dupG |
CLNSRC | |
CLNACC | RCV000059339.2, RCV000363659.1, |