rs370382601
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs370382601(A;G) |
Make rs370382601(G;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 16 |
Position | 89100682 |
Gene | ACSF3 |
is a | snp |
is | mentioned by |
dbSNP | rs370382601 |
dbSNP (classic) | rs370382601 |
ClinGen | rs370382601 |
ebi | rs370382601 |
HLI | rs370382601 |
Exac | rs370382601 |
Gnomad | rs370382601 |
Varsome | rs370382601 |
LitVar | rs370382601 |
Map | rs370382601 |
PheGenI | rs370382601 |
Biobank | rs370382601 |
1000 genomes | rs370382601 |
hgdp | rs370382601 |
ensembl | rs370382601 |
geneview | rs370382601 |
scholar | rs370382601 |
rs370382601 | |
pharmgkb | rs370382601 |
gwascentral | rs370382601 |
openSNP | rs370382601 |
23andMe | rs370382601 |
SNPshot | rs370382601 |
SNPdbe | rs370382601 |
MSV3d | rs370382601 |
GWAS Ctlg | rs370382601 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs370382601(G;G) |
Alt | rs370382601(G;G) |
Reference | Rs370382601(A;A) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ACSF3 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000016.9:g.89167090A>G |
CLNSRC | |
CLNACC | RCV000185752.1, |