rs33997857
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common on affy axiom data |
Make rs33997857(C;T) |
Make rs33997857(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 2 |
Position | 11787112 |
Gene | LPIN1 |
is a | snp |
is | mentioned by |
dbSNP | rs33997857 |
dbSNP (classic) | rs33997857 |
ClinGen | rs33997857 |
ebi | rs33997857 |
HLI | rs33997857 |
Exac | rs33997857 |
Gnomad | rs33997857 |
Varsome | rs33997857 |
LitVar | rs33997857 |
Map | rs33997857 |
PheGenI | rs33997857 |
Biobank | rs33997857 |
1000 genomes | rs33997857 |
hgdp | rs33997857 |
ensembl | rs33997857 |
geneview | rs33997857 |
scholar | rs33997857 |
rs33997857 | |
pharmgkb | rs33997857 |
gwascentral | rs33997857 |
openSNP | rs33997857 |
23andMe | rs33997857 |
SNPshot | rs33997857 |
SNPdbe | rs33997857 |
MSV3d | rs33997857 |
GWAS Ctlg | rs33997857 |
GMAF | 0.01102 |
Max Magnitude | 0 |
[PMID 20356931] Studies of association between LPIN1 variants and common metabolic phenotypes among 17,538 Danes
[PMID 18591397] Evaluating the role of LPIN1 variation in insulin resistance, body weight, and human lipodystrophy in U.K. Populations.
ClinVar | |
---|---|
Risk | rs33997857(A;A) rs33997857(T;T) |
Alt | rs33997857(A;A) rs33997857(T;T) |
Reference | Rs33997857(C;C) |
Significance | Probable-non-pathogenic |
Disease | not specified Acute Recurrent Myoglobinuria |
Variation | info |
Gene | LPIN1 |
CLNDBN | not specified Acute Recurrent Myoglobinuria |
Reversed | 1 |
HGVS | NC_000002.11:g.11927238G>A |
CLNSRC | |
CLNACC | RCV000252145.1, RCV000355477.1, |