rs58695352
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs58695352(C;T) |
Make rs58695352(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 16154755 |
Gene | ABCC6 |
is a | snp |
is | mentioned by |
dbSNP | rs58695352 |
dbSNP (classic) | rs58695352 |
ClinGen | rs58695352 |
ebi | rs58695352 |
HLI | rs58695352 |
Exac | rs58695352 |
Gnomad | rs58695352 |
Varsome | rs58695352 |
LitVar | rs58695352 |
Map | rs58695352 |
PheGenI | rs58695352 |
Biobank | rs58695352 |
1000 genomes | rs58695352 |
hgdp | rs58695352 |
ensembl | rs58695352 |
geneview | rs58695352 |
scholar | rs58695352 |
rs58695352 | |
pharmgkb | rs58695352 |
gwascentral | rs58695352 |
openSNP | rs58695352 |
23andMe | rs58695352 |
SNPshot | rs58695352 |
SNPdbe | rs58695352 |
MSV3d | rs58695352 |
GWAS Ctlg | rs58695352 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs58695352(T;T) |
Alt | rs58695352(T;T) |
Reference | Rs58695352(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ABCC6 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000016.9:g.16248612C>T |
CLNSRC | |
CLNACC | RCV000483462.1, |
[PMID 11536079] A spectrum of ABCC6 mutations is responsible for pseudoxanthoma elasticum.