rs587777833
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs587777833(C;C) |
Make rs587777833(C;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 12 |
Position | 14842968 |
Gene | ART4 |
is a | snp |
is | mentioned by |
dbSNP | rs587777833 |
dbSNP (classic) | rs587777833 |
ClinGen | rs587777833 |
ebi | rs587777833 |
HLI | rs587777833 |
Exac | rs587777833 |
Gnomad | rs587777833 |
Varsome | rs587777833 |
LitVar | rs587777833 |
Map | rs587777833 |
PheGenI | rs587777833 |
Biobank | rs587777833 |
1000 genomes | rs587777833 |
hgdp | rs587777833 |
ensembl | rs587777833 |
geneview | rs587777833 |
scholar | rs587777833 |
rs587777833 | |
pharmgkb | rs587777833 |
gwascentral | rs587777833 |
openSNP | rs587777833 |
23andMe | rs587777833 |
SNPshot | rs587777833 |
SNPdbe | rs587777833 |
MSV3d | rs587777833 |
GWAS Ctlg | rs587777833 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587777833(C;C) |
Alt | rs587777833(C;C) |
Reference | Rs587777833(T;T) |
Significance | Other |
Disease | Blood group |
Variation | info |
Gene | ART4 |
CLNDBN | Blood group, Dombrock system |
Reversed | 1 |
HGVS | NC_000012.11:g.14995902A>G |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000019307.25, |