rs886041906
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Chromosome | 2 |
Position | 203868002 |
Gene | CTLA4 |
is a | snp |
is | mentioned by |
dbSNP | rs886041906 |
dbSNP (classic) | rs886041906 |
ClinGen | rs886041906 |
ebi | rs886041906 |
HLI | rs886041906 |
Exac | rs886041906 |
Gnomad | rs886041906 |
Varsome | rs886041906 |
LitVar | rs886041906 |
Map | rs886041906 |
PheGenI | rs886041906 |
Biobank | rs886041906 |
1000 genomes | rs886041906 |
hgdp | rs886041906 |
ensembl | rs886041906 |
geneview | rs886041906 |
scholar | rs886041906 |
rs886041906 | |
pharmgkb | rs886041906 |
gwascentral | rs886041906 |
openSNP | rs886041906 |
23andMe | rs886041906 |
SNPshot | rs886041906 |
SNPdbe | rs886041906 |
MSV3d | rs886041906 |
GWAS Ctlg | rs886041906 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs886041906(A;A) |
Alt | rs886041906(A;A) |
Reference | Rs886041906(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | CTLA4 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.204732725G>A |
CLNSRC | |
CLNACC | RCV000274542.1, |