rs587777642
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(TCCCACCCTGGCAAAGC;TCCCACCCTGGCAAAGC) | 0 | common in clinvar |
Make rs587777642(-;-) |
Make rs587777642(-;ACCCTGGCAAAGCTCCC) |
Make rs587777642(ACCCTGGCAAAGCTCCC;ACCCTGGCAAAGCTCCC) |
Reference | GRCh38 38.1/142 |
Chromosome | 8 |
Position | 143215380 |
Gene | GPIHBP1 |
is a | snp |
is | mentioned by |
dbSNP | rs587777642 |
dbSNP (classic) | rs587777642 |
ClinGen | rs587777642 |
ebi | rs587777642 |
HLI | rs587777642 |
Exac | rs587777642 |
Gnomad | rs587777642 |
Varsome | rs587777642 |
LitVar | rs587777642 |
Map | rs587777642 |
PheGenI | rs587777642 |
Biobank | rs587777642 |
1000 genomes | rs587777642 |
hgdp | rs587777642 |
ensembl | rs587777642 |
geneview | rs587777642 |
scholar | rs587777642 |
rs587777642 | |
pharmgkb | rs587777642 |
gwascentral | rs587777642 |
openSNP | rs587777642 |
23andMe | rs587777642 |
SNPshot | rs587777642 |
SNPdbe | rs587777642 |
MSV3d | rs587777642 |
GWAS Ctlg | rs587777642 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587777642(-;-) |
Alt | rs587777642(-;-) |
Reference | Rs587777642(TCCCACCCTGGCAAAGC;TCCCACCCTGGCAAAGC) |
Significance | Pathogenic |
Disease | Hyperlipoproteinemia |
Variation | info |
Gene | GPIHBP1 |
CLNDBN | Hyperlipoproteinemia, type ID |
Reversed | 0 |
HGVS | NC_000008.10:g.144297255_144297271del17 |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000133528.3, |