rs761573352
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs761573352(A;A) |
Make rs761573352(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 16 |
Position | 89101270 |
Gene | ACSF3 |
is a | snp |
is | mentioned by |
dbSNP | rs761573352 |
dbSNP (classic) | rs761573352 |
ClinGen | rs761573352 |
ebi | rs761573352 |
HLI | rs761573352 |
Exac | rs761573352 |
Gnomad | rs761573352 |
Varsome | rs761573352 |
LitVar | rs761573352 |
Map | rs761573352 |
PheGenI | rs761573352 |
Biobank | rs761573352 |
1000 genomes | rs761573352 |
hgdp | rs761573352 |
ensembl | rs761573352 |
geneview | rs761573352 |
scholar | rs761573352 |
rs761573352 | |
pharmgkb | rs761573352 |
gwascentral | rs761573352 |
openSNP | rs761573352 |
23andMe | rs761573352 |
SNPshot | rs761573352 |
SNPdbe | rs761573352 |
MSV3d | rs761573352 |
GWAS Ctlg | rs761573352 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs761573352(A;A) |
Alt | rs761573352(A;A) |
Reference | Rs761573352(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ACSF3 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000016.9:g.89167678G>A |
CLNSRC | |
CLNACC | RCV000185756.1, |