rs869320669
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs869320669(A;A) |
Make rs869320669(A;C) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 10 |
Position | 125823225 |
Gene | BCCIP, UROS |
is a | snp |
is | mentioned by |
dbSNP | rs869320669 |
dbSNP (classic) | rs869320669 |
ClinGen | rs869320669 |
ebi | rs869320669 |
HLI | rs869320669 |
Exac | rs869320669 |
Gnomad | rs869320669 |
Varsome | rs869320669 |
LitVar | rs869320669 |
Map | rs869320669 |
PheGenI | rs869320669 |
Biobank | rs869320669 |
1000 genomes | rs869320669 |
hgdp | rs869320669 |
ensembl | rs869320669 |
geneview | rs869320669 |
scholar | rs869320669 |
rs869320669 | |
pharmgkb | rs869320669 |
gwascentral | rs869320669 |
openSNP | rs869320669 |
23andMe | rs869320669 |
SNPshot | rs869320669 |
SNPdbe | rs869320669 |
MSV3d | rs869320669 |
GWAS Ctlg | rs869320669 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs869320669(A;A) |
Alt | rs869320669(A;A) |
Reference | Rs869320669(C;C) |
Significance | Pathogenic |
Disease | Congenital erythropoietic porphyria |
Variation | info |
Gene | BCCIP UROS |
CLNDBN | Congenital erythropoietic porphyria |
Reversed | 1 |
HGVS | NC_000010.10:g.127511794G>T |
CLNSRC | |
CLNACC | RCV000210863.1, |