rs863224077
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(GT;GT) | 0 | common in clinvar |
Make rs863224077(-;-) |
Make rs863224077(-;TG) |
Make rs863224077(TG;TG) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 3 |
Position | 139352682 |
Gene | MRPS22 |
is a | snp |
is | mentioned by |
dbSNP | rs863224077 |
dbSNP (classic) | rs863224077 |
ClinGen | rs863224077 |
ebi | rs863224077 |
HLI | rs863224077 |
Exac | rs863224077 |
Gnomad | rs863224077 |
Varsome | rs863224077 |
LitVar | rs863224077 |
Map | rs863224077 |
PheGenI | rs863224077 |
Biobank | rs863224077 |
1000 genomes | rs863224077 |
hgdp | rs863224077 |
ensembl | rs863224077 |
geneview | rs863224077 |
scholar | rs863224077 |
rs863224077 | |
pharmgkb | rs863224077 |
gwascentral | rs863224077 |
openSNP | rs863224077 |
23andMe | rs863224077 |
SNPshot | rs863224077 |
SNPdbe | rs863224077 |
MSV3d | rs863224077 |
GWAS Ctlg | rs863224077 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs863224077(-;-) |
Alt | rs863224077(-;-) |
Reference | Rs863224077(GT;GT) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | MRPS22 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000003.11:g.139071524_139071525delTG |
CLNSRC | |
CLNACC | RCV000199847.1, |