rs72664281
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs72664281(A;A) |
Make rs72664281(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 16214375 |
Gene | ABCC6, LOC105371100 |
is a | snp |
is | mentioned by |
dbSNP | rs72664281 |
dbSNP (classic) | rs72664281 |
ClinGen | rs72664281 |
ebi | rs72664281 |
HLI | rs72664281 |
Exac | rs72664281 |
Gnomad | rs72664281 |
Varsome | rs72664281 |
LitVar | rs72664281 |
Map | rs72664281 |
PheGenI | rs72664281 |
Biobank | rs72664281 |
1000 genomes | rs72664281 |
hgdp | rs72664281 |
ensembl | rs72664281 |
geneview | rs72664281 |
scholar | rs72664281 |
rs72664281 | |
pharmgkb | rs72664281 |
gwascentral | rs72664281 |
openSNP | rs72664281 |
23andMe | rs72664281 |
SNPshot | rs72664281 |
SNPdbe | rs72664281 |
MSV3d | rs72664281 |
GWAS Ctlg | rs72664281 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs72664281(A;A) |
Alt | rs72664281(A;A) |
Reference | Rs72664281(G;G) |
Significance | Untested |
Disease | |
Variation | info |
Gene | ABCC6 |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000016.9:g.16308232C>T |
CLNSRC | |
CLNACC |
[PMID 10835642] Mutations in a gene encoding an ABC transporter cause pseudoxanthoma elasticum.