rs144334794
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs144334794(C;C) |
Make rs144334794(C;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 2 |
Position | 223963830 |
Gene | MRPL44 |
is a | snp |
is | mentioned by |
dbSNP | rs144334794 |
dbSNP (classic) | rs144334794 |
ClinGen | rs144334794 |
ebi | rs144334794 |
HLI | rs144334794 |
Exac | rs144334794 |
Gnomad | rs144334794 |
Varsome | rs144334794 |
LitVar | rs144334794 |
Map | rs144334794 |
PheGenI | rs144334794 |
Biobank | rs144334794 |
1000 genomes | rs144334794 |
hgdp | rs144334794 |
ensembl | rs144334794 |
geneview | rs144334794 |
scholar | rs144334794 |
rs144334794 | |
pharmgkb | rs144334794 |
gwascentral | rs144334794 |
openSNP | rs144334794 |
23andMe | rs144334794 |
SNPshot | rs144334794 |
SNPdbe | rs144334794 |
MSV3d | rs144334794 |
GWAS Ctlg | rs144334794 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs144334794(C;C) rs144334794(T;T) |
Alt | rs144334794(C;C) rs144334794(T;T) |
Reference | Rs144334794(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | MRPL44 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.224828547G>C |
CLNSRC | |
CLNACC | RCV000200219.1, |