rs372895468
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs372895468(C;T) |
Make rs372895468(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 22 |
Position | 40365037 |
Gene | ADSL |
is a | snp |
is | mentioned by |
dbSNP | rs372895468 |
dbSNP (classic) | rs372895468 |
ClinGen | rs372895468 |
ebi | rs372895468 |
HLI | rs372895468 |
Exac | rs372895468 |
Gnomad | rs372895468 |
Varsome | rs372895468 |
LitVar | rs372895468 |
Map | rs372895468 |
PheGenI | rs372895468 |
Biobank | rs372895468 |
1000 genomes | rs372895468 |
hgdp | rs372895468 |
ensembl | rs372895468 |
geneview | rs372895468 |
scholar | rs372895468 |
rs372895468 | |
pharmgkb | rs372895468 |
gwascentral | rs372895468 |
openSNP | rs372895468 |
23andMe | rs372895468 |
SNPshot | rs372895468 |
SNPdbe | rs372895468 |
MSV3d | rs372895468 |
GWAS Ctlg | rs372895468 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs372895468(G;G) rs372895468(T;T) |
Alt | rs372895468(G;G) rs372895468(T;T) |
Reference | Rs372895468(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ADSL |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000022.10:g.40761041C>G |
CLNSRC | UniProtKB (protein) |
CLNACC | RCV000186712.1, |