rs552120721
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs552120721(-;-) |
Make rs552120721(-;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 2 |
Position | 99162326 |
Gene | LIPT1, MITD1 |
is a | snp |
is | mentioned by |
dbSNP | rs552120721 |
dbSNP (classic) | rs552120721 |
ClinGen | rs552120721 |
ebi | rs552120721 |
HLI | rs552120721 |
Exac | rs552120721 |
Gnomad | rs552120721 |
Varsome | rs552120721 |
LitVar | rs552120721 |
Map | rs552120721 |
PheGenI | rs552120721 |
Biobank | rs552120721 |
1000 genomes | rs552120721 |
hgdp | rs552120721 |
ensembl | rs552120721 |
geneview | rs552120721 |
scholar | rs552120721 |
rs552120721 | |
pharmgkb | rs552120721 |
gwascentral | rs552120721 |
openSNP | rs552120721 |
23andMe | rs552120721 |
SNPshot | rs552120721 |
SNPdbe | rs552120721 |
MSV3d | rs552120721 |
GWAS Ctlg | rs552120721 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs552120721(-;-) |
Alt | rs552120721(-;-) |
Reference | Rs552120721(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | LIPT1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.99778789delG |
CLNSRC | |
CLNACC | RCV000483728.1, |