rs72653792
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs72653792(G;T) |
Make rs72653792(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 16 |
Position | 16178854 |
Gene | ABCC6 |
is a | snp |
is | mentioned by |
dbSNP | rs72653792 |
dbSNP (classic) | rs72653792 |
ClinGen | rs72653792 |
ebi | rs72653792 |
HLI | rs72653792 |
Exac | rs72653792 |
Gnomad | rs72653792 |
Varsome | rs72653792 |
LitVar | rs72653792 |
Map | rs72653792 |
PheGenI | rs72653792 |
Biobank | rs72653792 |
1000 genomes | rs72653792 |
hgdp | rs72653792 |
ensembl | rs72653792 |
geneview | rs72653792 |
scholar | rs72653792 |
rs72653792 | |
pharmgkb | rs72653792 |
gwascentral | rs72653792 |
openSNP | rs72653792 |
23andMe | rs72653792 |
SNPshot | rs72653792 |
SNPdbe | rs72653792 |
MSV3d | rs72653792 |
GWAS Ctlg | rs72653792 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs72653792(A;A) rs72653792(T;T) |
Alt | rs72653792(A;A) rs72653792(T;T) |
Reference | Rs72653792(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ABCC6 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000016.9:g.16272711C>T |
CLNSRC | |
CLNACC | RCV000483030.1, |