rs121912502
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs121912502(C;T) |
Make rs121912502(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 15 |
Position | 58548387 |
Gene | LIPC |
is a | snp |
is | mentioned by |
dbSNP | rs121912502 |
dbSNP (classic) | rs121912502 |
ClinGen | rs121912502 |
ebi | rs121912502 |
HLI | rs121912502 |
Exac | rs121912502 |
Gnomad | rs121912502 |
Varsome | rs121912502 |
LitVar | rs121912502 |
Map | rs121912502 |
PheGenI | rs121912502 |
Biobank | rs121912502 |
1000 genomes | rs121912502 |
hgdp | rs121912502 |
ensembl | rs121912502 |
geneview | rs121912502 |
scholar | rs121912502 |
rs121912502 | |
pharmgkb | rs121912502 |
gwascentral | rs121912502 |
openSNP | rs121912502 |
23andMe | rs121912502 |
SNPshot | rs121912502 |
SNPdbe | rs121912502 |
MSV3d | rs121912502 |
GWAS Ctlg | rs121912502 |
GMAF | 0.0004591 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121912502(T;T) |
Alt | rs121912502(T;T) |
Reference | Rs121912502(C;C) |
Significance | Other |
Disease | Hepatic lipase deficiency |
Variation | info |
Gene | LIPC |
CLNDBN | Hepatic lipase deficiency |
Reversed | 0 |
HGVS | NC_000015.9:g.58840586C>T |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000015537.25, |