rs138228629
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs138228629(A;A) |
Make rs138228629(A;G) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 13 |
Position | 24906342 |
Gene | CENPJ |
is a | snp |
is | mentioned by |
dbSNP | rs138228629 |
dbSNP (classic) | rs138228629 |
ClinGen | rs138228629 |
ebi | rs138228629 |
HLI | rs138228629 |
Exac | rs138228629 |
Gnomad | rs138228629 |
Varsome | rs138228629 |
LitVar | rs138228629 |
Map | rs138228629 |
PheGenI | rs138228629 |
Biobank | rs138228629 |
1000 genomes | rs138228629 |
hgdp | rs138228629 |
ensembl | rs138228629 |
geneview | rs138228629 |
scholar | rs138228629 |
rs138228629 | |
pharmgkb | rs138228629 |
gwascentral | rs138228629 |
openSNP | rs138228629 |
23andMe | rs138228629 |
SNPshot | rs138228629 |
SNPdbe | rs138228629 |
MSV3d | rs138228629 |
GWAS Ctlg | rs138228629 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs138228629(A;A) |
Alt | rs138228629(A;A) |
Reference | Rs138228629(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | CENPJ |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000013.10:g.25480480G>A |
CLNSRC | |
CLNACC | RCV000369854.1, |