rs751342087
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs751342087(-;G) |
Make rs751342087(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 16 |
Position | 89145276 |
Gene | ACSF3 |
is a | snp |
is | mentioned by |
dbSNP | rs751342087 |
dbSNP (classic) | rs751342087 |
ClinGen | rs751342087 |
ebi | rs751342087 |
HLI | rs751342087 |
Exac | rs751342087 |
Gnomad | rs751342087 |
Varsome | rs751342087 |
LitVar | rs751342087 |
Map | rs751342087 |
PheGenI | rs751342087 |
Biobank | rs751342087 |
1000 genomes | rs751342087 |
hgdp | rs751342087 |
ensembl | rs751342087 |
geneview | rs751342087 |
scholar | rs751342087 |
rs751342087 | |
pharmgkb | rs751342087 |
gwascentral | rs751342087 |
openSNP | rs751342087 |
23andMe | rs751342087 |
SNPshot | rs751342087 |
SNPdbe | rs751342087 |
MSV3d | rs751342087 |
GWAS Ctlg | rs751342087 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs751342087(G;G) |
Alt | rs751342087(G;G) |
Reference | Rs751342087(-;-) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | ACSF3 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000016.9:g.89211686dup |
CLNSRC | |
CLNACC | RCV000489924.2, |