rs752104014
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs752104014(A;A) |
Make rs752104014(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 16 |
Position | 89102643 |
Gene | ACSF3 |
is a | snp |
is | mentioned by |
dbSNP | rs752104014 |
dbSNP (classic) | rs752104014 |
ClinGen | rs752104014 |
ebi | rs752104014 |
HLI | rs752104014 |
Exac | rs752104014 |
Gnomad | rs752104014 |
Varsome | rs752104014 |
LitVar | rs752104014 |
Map | rs752104014 |
PheGenI | rs752104014 |
Biobank | rs752104014 |
1000 genomes | rs752104014 |
hgdp | rs752104014 |
ensembl | rs752104014 |
geneview | rs752104014 |
scholar | rs752104014 |
rs752104014 | |
pharmgkb | rs752104014 |
gwascentral | rs752104014 |
openSNP | rs752104014 |
23andMe | rs752104014 |
SNPshot | rs752104014 |
SNPdbe | rs752104014 |
MSV3d | rs752104014 |
GWAS Ctlg | rs752104014 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs752104014(A;A) |
Alt | rs752104014(A;A) |
Reference | Rs752104014(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | ACSF3 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000016.9:g.89169051G>A |
CLNSRC | |
CLNACC | RCV000185758.1, |