rs763481375
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs763481375(A;A) |
Make rs763481375(A;G) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 2 |
Position | 215011631 |
Gene | ABCA12 |
is a | snp |
is | mentioned by |
dbSNP | rs763481375 |
dbSNP (classic) | rs763481375 |
ClinGen | rs763481375 |
ebi | rs763481375 |
HLI | rs763481375 |
Exac | rs763481375 |
Gnomad | rs763481375 |
Varsome | rs763481375 |
LitVar | rs763481375 |
Map | rs763481375 |
PheGenI | rs763481375 |
Biobank | rs763481375 |
1000 genomes | rs763481375 |
hgdp | rs763481375 |
ensembl | rs763481375 |
geneview | rs763481375 |
scholar | rs763481375 |
rs763481375 | |
pharmgkb | rs763481375 |
gwascentral | rs763481375 |
openSNP | rs763481375 |
23andMe | rs763481375 |
SNPshot | rs763481375 |
SNPdbe | rs763481375 |
MSV3d | rs763481375 |
GWAS Ctlg | rs763481375 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs763481375(A;A) |
Alt | rs763481375(A;A) |
Reference | Rs763481375(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ABCA12 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.215876355G>A |
CLNSRC | |
CLNACC | RCV000256167.1, |