rs863224251
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs863224251(A;T) |
Make rs863224251(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 22 |
Position | 50528552 |
Gene | TYMP |
is a | snp |
is | mentioned by |
dbSNP | rs863224251 |
dbSNP (classic) | rs863224251 |
ClinGen | rs863224251 |
ebi | rs863224251 |
HLI | rs863224251 |
Exac | rs863224251 |
Gnomad | rs863224251 |
Varsome | rs863224251 |
LitVar | rs863224251 |
Map | rs863224251 |
PheGenI | rs863224251 |
Biobank | rs863224251 |
1000 genomes | rs863224251 |
hgdp | rs863224251 |
ensembl | rs863224251 |
geneview | rs863224251 |
scholar | rs863224251 |
rs863224251 | |
pharmgkb | rs863224251 |
gwascentral | rs863224251 |
openSNP | rs863224251 |
23andMe | rs863224251 |
SNPshot | rs863224251 |
SNPdbe | rs863224251 |
MSV3d | rs863224251 |
GWAS Ctlg | rs863224251 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs863224251(T;T) |
Alt | rs863224251(T;T) |
Reference | Rs863224251(A;A) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | TYMP |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000022.10:g.50966981T>A |
CLNSRC | |
CLNACC | RCV000200518.1, |