rs147739245
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs147739245(C;T) |
Make rs147739245(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 3 |
Position | 139352701 |
Gene | MRPS22 |
is a | snp |
is | mentioned by |
dbSNP | rs147739245 |
dbSNP (classic) | rs147739245 |
ClinGen | rs147739245 |
ebi | rs147739245 |
HLI | rs147739245 |
Exac | rs147739245 |
Gnomad | rs147739245 |
Varsome | rs147739245 |
LitVar | rs147739245 |
Map | rs147739245 |
PheGenI | rs147739245 |
Biobank | rs147739245 |
1000 genomes | rs147739245 |
hgdp | rs147739245 |
ensembl | rs147739245 |
geneview | rs147739245 |
scholar | rs147739245 |
rs147739245 | |
pharmgkb | rs147739245 |
gwascentral | rs147739245 |
openSNP | rs147739245 |
23andMe | rs147739245 |
SNPshot | rs147739245 |
SNPdbe | rs147739245 |
MSV3d | rs147739245 |
GWAS Ctlg | rs147739245 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs147739245(T;T) |
Alt | rs147739245(T;T) |
Reference | Rs147739245(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | MRPS22 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000003.11:g.139071543C>T |
CLNSRC | |
CLNACC | RCV000198671.1, |