rs587776824
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(GGGCGGGCGGCGGCGGCGGCA;GGGCGGGCGGCGGCGGCGGCA) | 0 | common in clinvar |
Make rs587776824(-;-) |
Make rs587776824(-;GGCGGGCGGCGGCGGCGGCAG) |
Make rs587776824(GGCGGGCGGCGGCGGCGGCAG;GGCGGGCGGCGGCGGCGGCAG) |
Reference | GRCh38 38.1/142 |
Chromosome | 2 |
Position | 176093054 |
Gene | HOXD13 |
is a | snp |
is | mentioned by |
dbSNP | rs587776824 |
dbSNP (classic) | rs587776824 |
ClinGen | rs587776824 |
ebi | rs587776824 |
HLI | rs587776824 |
Exac | rs587776824 |
Gnomad | rs587776824 |
Varsome | rs587776824 |
LitVar | rs587776824 |
Map | rs587776824 |
PheGenI | rs587776824 |
Biobank | rs587776824 |
1000 genomes | rs587776824 |
hgdp | rs587776824 |
ensembl | rs587776824 |
geneview | rs587776824 |
scholar | rs587776824 |
rs587776824 | |
pharmgkb | rs587776824 |
gwascentral | rs587776824 |
openSNP | rs587776824 |
23andMe | rs587776824 |
SNPshot | rs587776824 |
SNPdbe | rs587776824 |
MSV3d | rs587776824 |
GWAS Ctlg | rs587776824 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587776824(-;-) |
Alt | rs587776824(-;-) |
Reference | Rs587776824(GGGCGGGCGGCGGCGGCGGCA;GGGCGGGCGGCGGCGGCGGCA) |
Significance | Pathogenic |
Disease | VACTERL association |
Variation | info |
Gene | HOXD13 |
CLNDBN | VACTERL association |
Reversed | 0 |
HGVS | NC_000002.11:g.176957782_176957802del21 |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000016005.28, |