rs398122988
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;CTCAA) | 5 | Lowered risk (0.6x) of coronary artery disease |
(AACTC;AACTC) | 0 | common in clinvar |
(CTCAA;CTCAA) | 0 | common in clinvar |
Make rs398122988(-;-) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 1 |
Position | 62597929 |
Gene | ANGPTL3, DOCK7 |
is a | snp |
is | mentioned by |
dbSNP | rs398122988 |
dbSNP (classic) | rs398122988 |
ClinGen | rs398122988 |
ebi | rs398122988 |
HLI | rs398122988 |
Exac | rs398122988 |
Gnomad | rs398122988 |
Varsome | rs398122988 |
LitVar | rs398122988 |
Map | rs398122988 |
PheGenI | rs398122988 |
Biobank | rs398122988 |
1000 genomes | rs398122988 |
hgdp | rs398122988 |
ensembl | rs398122988 |
geneview | rs398122988 |
scholar | rs398122988 |
rs398122988 | |
pharmgkb | rs398122988 |
gwascentral | rs398122988 |
openSNP | rs398122988 |
23andMe | rs398122988 |
SNPshot | rs398122988 |
SNPdbe | rs398122988 |
MSV3d | rs398122988 |
GWAS Ctlg | rs398122988 |
Merged from | Rs569107562 |
Max Magnitude | 5 |
ANGPTL3, c.363_367delCTCAA (p.Asn121Lysfs)
ClinVar | |
---|---|
Risk | rs398122988(-;-) Rs398122988(AACTC;AACTC) |
Alt | rs398122988(-;-) Rs398122988(AACTC;AACTC) |
Reference | Rs398122988(CTCAA;CTCAA) |
Significance | Pathogenic |
Disease | Hypobetalipoproteinemia |
Variation | info |
Gene | DOCK7 ANGPTL3 |
CLNDBN | Hypobetalipoproteinemia, familial, 2 |
Reversed | 0 |
HGVS | NC_000001.10:g.63063600_63063604delCTCAA |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000077769.2, |