rs756933588
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs756933588(C;T) |
Make rs756933588(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 18 |
Position | 2929065 |
Gene | LPIN2 |
is a | snp |
is | mentioned by |
dbSNP | rs756933588 |
dbSNP (classic) | rs756933588 |
ClinGen | rs756933588 |
ebi | rs756933588 |
HLI | rs756933588 |
Exac | rs756933588 |
Gnomad | rs756933588 |
Varsome | rs756933588 |
LitVar | rs756933588 |
Map | rs756933588 |
PheGenI | rs756933588 |
Biobank | rs756933588 |
1000 genomes | rs756933588 |
hgdp | rs756933588 |
ensembl | rs756933588 |
geneview | rs756933588 |
scholar | rs756933588 |
rs756933588 | |
pharmgkb | rs756933588 |
gwascentral | rs756933588 |
openSNP | rs756933588 |
23andMe | rs756933588 |
SNPshot | rs756933588 |
SNPdbe | rs756933588 |
MSV3d | rs756933588 |
GWAS Ctlg | rs756933588 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs756933588(T;T) |
Alt | rs756933588(T;T) |
Reference | Rs756933588(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | LPIN2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000018.9:g.2929063C>T |
CLNSRC | |
CLNACC | RCV000217293.1, |