rs72549389
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs72549389(C;C) |
Make rs72549389(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 38075387 |
Gene | CYP1B1 |
is a | snp |
is | mentioned by |
dbSNP | rs72549389 |
dbSNP (classic) | rs72549389 |
ClinGen | rs72549389 |
ebi | rs72549389 |
HLI | rs72549389 |
Exac | rs72549389 |
Gnomad | rs72549389 |
Varsome | rs72549389 |
LitVar | rs72549389 |
Map | rs72549389 |
PheGenI | rs72549389 |
Biobank | rs72549389 |
1000 genomes | rs72549389 |
hgdp | rs72549389 |
ensembl | rs72549389 |
geneview | rs72549389 |
scholar | rs72549389 |
rs72549389 | |
pharmgkb | rs72549389 |
gwascentral | rs72549389 |
openSNP | rs72549389 |
23andMe | rs72549389 |
SNPshot | rs72549389 |
SNPdbe | rs72549389 |
MSV3d | rs72549389 |
GWAS Ctlg | rs72549389 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs72549389(C;C) |
Alt | rs72549389(C;C) |
Reference | Rs72549389(T;T) |
Significance | Pathogenic |
Disease | Anterior segment dysgenesis 6 |
Variation | info |
Gene | CYP1B1 |
CLNDBN | Anterior segment dysgenesis 6 |
Reversed | 1 |
HGVS | NC_000002.11:g.38302530A>G |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000008175.4, |