rs758753966
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs758753966(A;C) |
Make rs758753966(C;C) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 1 |
Position | 75761120 |
Gene | ACADM |
is a | snp |
is | mentioned by |
dbSNP | rs758753966 |
dbSNP (classic) | rs758753966 |
ClinGen | rs758753966 |
ebi | rs758753966 |
HLI | rs758753966 |
Exac | rs758753966 |
Gnomad | rs758753966 |
Varsome | rs758753966 |
LitVar | rs758753966 |
Map | rs758753966 |
PheGenI | rs758753966 |
Biobank | rs758753966 |
1000 genomes | rs758753966 |
hgdp | rs758753966 |
ensembl | rs758753966 |
geneview | rs758753966 |
scholar | rs758753966 |
rs758753966 | |
pharmgkb | rs758753966 |
gwascentral | rs758753966 |
openSNP | rs758753966 |
23andMe | rs758753966 |
SNPshot | rs758753966 |
SNPdbe | rs758753966 |
MSV3d | rs758753966 |
GWAS Ctlg | rs758753966 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs758753966(C;C) |
Alt | rs758753966(C;C) |
Reference | Rs758753966(A;A) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ACADM |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.76226805A>C |
CLNSRC | |
CLNACC | RCV000255491.1, |