rs587777831
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs587777831(A;G) |
Make rs587777831(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 12 |
Position | 14841155 |
Gene | ART4 |
is a | snp |
is | mentioned by |
dbSNP | rs587777831 |
dbSNP (classic) | rs587777831 |
ClinGen | rs587777831 |
ebi | rs587777831 |
HLI | rs587777831 |
Exac | rs587777831 |
Gnomad | rs587777831 |
Varsome | rs587777831 |
LitVar | rs587777831 |
Map | rs587777831 |
PheGenI | rs587777831 |
Biobank | rs587777831 |
1000 genomes | rs587777831 |
hgdp | rs587777831 |
ensembl | rs587777831 |
geneview | rs587777831 |
scholar | rs587777831 |
rs587777831 | |
pharmgkb | rs587777831 |
gwascentral | rs587777831 |
openSNP | rs587777831 |
23andMe | rs587777831 |
SNPshot | rs587777831 |
SNPdbe | rs587777831 |
MSV3d | rs587777831 |
GWAS Ctlg | rs587777831 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587777831(G;G) |
Alt | rs587777831(G;G) |
Reference | Rs587777831(A;A) |
Significance | Other |
Disease | Blood group |
Variation | info |
Gene | ART4 |
CLNDBN | Blood group, Dombrock system |
Reversed | 1 |
HGVS | NC_000012.11:g.14994089T>C |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000019305.25, |