rs587776507
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(CCTGGCTGGCCTGT;CCTGGCTGGCCTGT) | 0 | common in clinvar |
Make rs587776507(-;-) |
Make rs587776507(-;TGGCCTGTCCTGGC) |
Make rs587776507(TGGCCTGTCCTGGC;TGGCCTGTCCTGGC) |
Reference | GRCh38 38.1/142 |
Chromosome | 1 |
Position | 159205725 |
Gene | ACKR1 |
is a | snp |
is | mentioned by |
dbSNP | rs587776507 |
dbSNP (classic) | rs587776507 |
ClinGen | rs587776507 |
ebi | rs587776507 |
HLI | rs587776507 |
Exac | rs587776507 |
Gnomad | rs587776507 |
Varsome | rs587776507 |
LitVar | rs587776507 |
Map | rs587776507 |
PheGenI | rs587776507 |
Biobank | rs587776507 |
1000 genomes | rs587776507 |
hgdp | rs587776507 |
ensembl | rs587776507 |
geneview | rs587776507 |
scholar | rs587776507 |
rs587776507 | |
pharmgkb | rs587776507 |
gwascentral | rs587776507 |
openSNP | rs587776507 |
23andMe | rs587776507 |
SNPshot | rs587776507 |
SNPdbe | rs587776507 |
MSV3d | rs587776507 |
GWAS Ctlg | rs587776507 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587776507(-;-) |
Alt | rs587776507(-;-) |
Reference | Rs587776507(CCTGGCTGGCCTGT;CCTGGCTGGCCTGT) |
Significance | Pathogenic |
Disease | DUFFY BLOOD GROUP SYSTEM |
Variation | info |
Gene | ACKR1 |
CLNDBN | DUFFY BLOOD GROUP SYSTEM, FY(a-b-) PHENOTYPE |
Reversed | 0 |
HGVS | NC_000001.10:g.159175515_159175528delTGGCCTGTCCTGGC |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000000010.3, |