rs72653706
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs72653706(C;T) |
Make rs72653706(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 16 |
Position | 16163078 |
Gene | ABCC6 |
is a | snp |
is | mentioned by |
dbSNP | rs72653706 |
dbSNP (classic) | rs72653706 |
ClinGen | rs72653706 |
ebi | rs72653706 |
HLI | rs72653706 |
Exac | rs72653706 |
Gnomad | rs72653706 |
Varsome | rs72653706 |
LitVar | rs72653706 |
Map | rs72653706 |
PheGenI | rs72653706 |
Biobank | rs72653706 |
1000 genomes | rs72653706 |
hgdp | rs72653706 |
ensembl | rs72653706 |
geneview | rs72653706 |
scholar | rs72653706 |
rs72653706 | |
pharmgkb | rs72653706 |
gwascentral | rs72653706 |
openSNP | rs72653706 |
23andMe | rs72653706 |
SNPshot | rs72653706 |
SNPdbe | rs72653706 |
MSV3d | rs72653706 |
GWAS Ctlg | rs72653706 |
GMAF | 0.001377 |
Max Magnitude | 0 |
aka c.3421C>T (p.Arg1141Ter or R1141X)
ClinVar | |
---|---|
Risk | rs72653706(T;T) |
Alt | rs72653706(T;T) |
Reference | Rs72653706(C;C) |
Significance | Pathogenic |
Disease | Pseudoxanthoma elasticum Generalized arterial calcification of infancy 2 not provided Pseudoxanthoma elasticum Cutis laxa Papule |
Variation | info |
Gene | ABCC6 |
CLNDBN | Pseudoxanthoma elasticum Generalized arterial calcification of infancy 2 not provided Pseudoxanthoma elasticum, forme fruste Cutis laxa Papule |
Reversed | 1 |
HGVS | NC_000016.9:g.16256935G>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000006937.5, RCV000023272.5, RCV000254838.2, RCV000280878.1, RCV000415101.1, |
[PMID 10835643] Mutations in ABCC6 cause pseudoxanthoma elasticum.