rs56340844
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs56340844(C;T) |
Make rs56340844(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 14840856 |
Gene | ART4 |
is a | snp |
is | mentioned by |
dbSNP | rs56340844 |
dbSNP (classic) | rs56340844 |
ClinGen | rs56340844 |
ebi | rs56340844 |
HLI | rs56340844 |
Exac | rs56340844 |
Gnomad | rs56340844 |
Varsome | rs56340844 |
LitVar | rs56340844 |
Map | rs56340844 |
PheGenI | rs56340844 |
Biobank | rs56340844 |
1000 genomes | rs56340844 |
hgdp | rs56340844 |
ensembl | rs56340844 |
geneview | rs56340844 |
scholar | rs56340844 |
rs56340844 | |
pharmgkb | rs56340844 |
gwascentral | rs56340844 |
openSNP | rs56340844 |
23andMe | rs56340844 |
SNPshot | rs56340844 |
SNPdbe | rs56340844 |
MSV3d | rs56340844 |
GWAS Ctlg | rs56340844 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs56340844(T;T) |
Alt | rs56340844(T;T) |
Reference | Rs56340844(C;C) |
Significance | Other |
Disease | Blood group |
Variation | info |
Gene | ART4 |
CLNDBN | Blood group, Dombrock system |
Reversed | 1 |
HGVS | NC_000012.11:g.14993790G>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000019308.29, |