rs747330606
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs747330606(G;T) |
Make rs747330606(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 22 |
Position | 41515536 |
Gene | ACO2 |
is a | snp |
is | mentioned by |
dbSNP | rs747330606 |
dbSNP (classic) | rs747330606 |
ClinGen | rs747330606 |
ebi | rs747330606 |
HLI | rs747330606 |
Exac | rs747330606 |
Gnomad | rs747330606 |
Varsome | rs747330606 |
LitVar | rs747330606 |
Map | rs747330606 |
PheGenI | rs747330606 |
Biobank | rs747330606 |
1000 genomes | rs747330606 |
hgdp | rs747330606 |
ensembl | rs747330606 |
geneview | rs747330606 |
scholar | rs747330606 |
rs747330606 | |
pharmgkb | rs747330606 |
gwascentral | rs747330606 |
openSNP | rs747330606 |
23andMe | rs747330606 |
SNPshot | rs747330606 |
SNPdbe | rs747330606 |
MSV3d | rs747330606 |
GWAS Ctlg | rs747330606 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs747330606(T;T) |
Alt | rs747330606(T;T) |
Reference | Rs747330606(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ACO2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000022.10:g.41911540G>T |
CLNSRC | |
CLNACC | RCV000200546.2, |