rs863224176
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs863224176(A;C) |
Make rs863224176(C;C) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 12 |
Position | 131941625 |
Gene | PUS1 |
is a | snp |
is | mentioned by |
dbSNP | rs863224176 |
dbSNP (classic) | rs863224176 |
ClinGen | rs863224176 |
ebi | rs863224176 |
HLI | rs863224176 |
Exac | rs863224176 |
Gnomad | rs863224176 |
Varsome | rs863224176 |
LitVar | rs863224176 |
Map | rs863224176 |
PheGenI | rs863224176 |
Biobank | rs863224176 |
1000 genomes | rs863224176 |
hgdp | rs863224176 |
ensembl | rs863224176 |
geneview | rs863224176 |
scholar | rs863224176 |
rs863224176 | |
pharmgkb | rs863224176 |
gwascentral | rs863224176 |
openSNP | rs863224176 |
23andMe | rs863224176 |
SNPshot | rs863224176 |
SNPdbe | rs863224176 |
MSV3d | rs863224176 |
GWAS Ctlg | rs863224176 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs863224176(C;C) |
Alt | rs863224176(C;C) |
Reference | Rs863224176(A;A) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | PUS1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000012.11:g.132426170A>C |
CLNSRC | |
CLNACC | RCV000195831.1, |