rs74315454
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs74315454(A;A) |
Make rs74315454(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 22 |
Position | 42693169 |
Gene | A4GALT |
is a | snp |
is | mentioned by |
dbSNP | rs74315454 |
dbSNP (classic) | rs74315454 |
ClinGen | rs74315454 |
ebi | rs74315454 |
HLI | rs74315454 |
Exac | rs74315454 |
Gnomad | rs74315454 |
Varsome | rs74315454 |
LitVar | rs74315454 |
Map | rs74315454 |
PheGenI | rs74315454 |
Biobank | rs74315454 |
1000 genomes | rs74315454 |
hgdp | rs74315454 |
ensembl | rs74315454 |
geneview | rs74315454 |
scholar | rs74315454 |
rs74315454 | |
pharmgkb | rs74315454 |
gwascentral | rs74315454 |
openSNP | rs74315454 |
23andMe | rs74315454 |
SNPshot | rs74315454 |
SNPdbe | rs74315454 |
MSV3d | rs74315454 |
GWAS Ctlg | rs74315454 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs74315454(A;A) rs74315454(C;C) |
Alt | rs74315454(A;A) rs74315454(C;C) |
Reference | Rs74315454(G;G) |
Significance | Other |
Disease | p phenotype |
Variation | info |
Gene | A4GALT |
CLNDBN | p phenotype |
Reversed | 1 |
HGVS | NC_000022.10:g.43089175C>T |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000002813.3, |