rs761557390
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs761557390(A;C) |
Make rs761557390(C;C) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 2 |
Position | 214966945 |
Gene | ABCA12 |
is a | snp |
is | mentioned by |
dbSNP | rs761557390 |
dbSNP (classic) | rs761557390 |
ClinGen | rs761557390 |
ebi | rs761557390 |
HLI | rs761557390 |
Exac | rs761557390 |
Gnomad | rs761557390 |
Varsome | rs761557390 |
LitVar | rs761557390 |
Map | rs761557390 |
PheGenI | rs761557390 |
Biobank | rs761557390 |
1000 genomes | rs761557390 |
hgdp | rs761557390 |
ensembl | rs761557390 |
geneview | rs761557390 |
scholar | rs761557390 |
rs761557390 | |
pharmgkb | rs761557390 |
gwascentral | rs761557390 |
openSNP | rs761557390 |
23andMe | rs761557390 |
SNPshot | rs761557390 |
SNPdbe | rs761557390 |
MSV3d | rs761557390 |
GWAS Ctlg | rs761557390 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs761557390(C;C) |
Alt | rs761557390(C;C) |
Reference | Rs761557390(A;A) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ABCA12 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.215831669A>C |
CLNSRC | |
CLNACC | RCV000276997.1, |