rs754287486
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs754287486(A;A) |
Make rs754287486(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 7 |
Position | 87452954 |
Gene | ABCB4 |
is a | snp |
is | mentioned by |
dbSNP | rs754287486 |
dbSNP (classic) | rs754287486 |
ClinGen | rs754287486 |
ebi | rs754287486 |
HLI | rs754287486 |
Exac | rs754287486 |
Gnomad | rs754287486 |
Varsome | rs754287486 |
LitVar | rs754287486 |
Map | rs754287486 |
PheGenI | rs754287486 |
Biobank | rs754287486 |
1000 genomes | rs754287486 |
hgdp | rs754287486 |
ensembl | rs754287486 |
geneview | rs754287486 |
scholar | rs754287486 |
rs754287486 | |
pharmgkb | rs754287486 |
gwascentral | rs754287486 |
openSNP | rs754287486 |
23andMe | rs754287486 |
SNPshot | rs754287486 |
SNPdbe | rs754287486 |
MSV3d | rs754287486 |
GWAS Ctlg | rs754287486 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs754287486(A;A) |
Alt | rs754287486(A;A) |
Reference | Rs754287486(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | ABCB4 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000007.13:g.87082270G>A |
CLNSRC | |
CLNACC | RCV000414549.1, |