rs747593459
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs747593459(G;G) |
Make rs747593459(G;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 1 |
Position | 75750527 |
Gene | ACADM |
is a | snp |
is | mentioned by |
dbSNP | rs747593459 |
dbSNP (classic) | rs747593459 |
ClinGen | rs747593459 |
ebi | rs747593459 |
HLI | rs747593459 |
Exac | rs747593459 |
Gnomad | rs747593459 |
Varsome | rs747593459 |
LitVar | rs747593459 |
Map | rs747593459 |
PheGenI | rs747593459 |
Biobank | rs747593459 |
1000 genomes | rs747593459 |
hgdp | rs747593459 |
ensembl | rs747593459 |
geneview | rs747593459 |
scholar | rs747593459 |
rs747593459 | |
pharmgkb | rs747593459 |
gwascentral | rs747593459 |
openSNP | rs747593459 |
23andMe | rs747593459 |
SNPshot | rs747593459 |
SNPdbe | rs747593459 |
MSV3d | rs747593459 |
GWAS Ctlg | rs747593459 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs747593459(G;G) |
Alt | rs747593459(G;G) |
Reference | Rs747593459(T;T) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | ACADM |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.76216212T>G |
CLNSRC | |
CLNACC | RCV000185678.1, |