rs398122855
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs398122855(C;C) |
Make rs398122855(C;G) |
Reference | GRCh38 38.1/141 |
Chromosome | X |
Position | 107642384 |
Gene | PRPS1 |
is a | snp |
is | mentioned by |
dbSNP | rs398122855 |
dbSNP (classic) | rs398122855 |
ClinGen | rs398122855 |
ebi | rs398122855 |
HLI | rs398122855 |
Exac | rs398122855 |
Gnomad | rs398122855 |
Varsome | rs398122855 |
LitVar | rs398122855 |
Map | rs398122855 |
PheGenI | rs398122855 |
Biobank | rs398122855 |
1000 genomes | rs398122855 |
hgdp | rs398122855 |
ensembl | rs398122855 |
geneview | rs398122855 |
scholar | rs398122855 |
rs398122855 | |
pharmgkb | rs398122855 |
gwascentral | rs398122855 |
openSNP | rs398122855 |
23andMe | rs398122855 |
SNPshot | rs398122855 |
SNPdbe | rs398122855 |
MSV3d | rs398122855 |
GWAS Ctlg | rs398122855 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs398122855(C;C) |
Alt | rs398122855(C;C) |
Reference | Rs398122855(G;G) |
Significance | Pathogenic |
Disease | Arts syndrome |
Variation | info |
Gene | PRPS1 |
CLNDBN | Arts syndrome |
Reversed | 0 |
HGVS | NC_000023.10:g.106885614G>C |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000022882.4, |