rs886037774
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs886037774(C;C) |
Make rs886037774(C;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 8 |
Position | 19955993 |
Gene | LPL |
is a | snp |
is | mentioned by |
dbSNP | rs886037774 |
dbSNP (classic) | rs886037774 |
ClinGen | rs886037774 |
ebi | rs886037774 |
HLI | rs886037774 |
Exac | rs886037774 |
Gnomad | rs886037774 |
Varsome | rs886037774 |
LitVar | rs886037774 |
Map | rs886037774 |
PheGenI | rs886037774 |
Biobank | rs886037774 |
1000 genomes | rs886037774 |
hgdp | rs886037774 |
ensembl | rs886037774 |
geneview | rs886037774 |
scholar | rs886037774 |
rs886037774 | |
pharmgkb | rs886037774 |
gwascentral | rs886037774 |
openSNP | rs886037774 |
23andMe | rs886037774 |
SNPshot | rs886037774 |
SNPdbe | rs886037774 |
MSV3d | rs886037774 |
GWAS Ctlg | rs886037774 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs886037774(C;C) |
Alt | rs886037774(C;C) |
Reference | Rs886037774(T;T) |
Significance | Probable-Pathogenic |
Disease | Hyperlipoproteinemia |
Variation | info |
Gene | LPL |
CLNDBN | Hyperlipoproteinemia, type I |
Reversed | 0 |
HGVS | NC_000008.10:g.19813504T>C |
CLNSRC | |
CLNACC | RCV000258506.1, |