rs727502787
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs727502787(A;G) |
Make rs727502787(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 10 |
Position | 102402267 |
Gene | NFKB2, PSD |
is a | snp |
is | mentioned by |
dbSNP | rs727502787 |
dbSNP (classic) | rs727502787 |
ClinGen | rs727502787 |
ebi | rs727502787 |
HLI | rs727502787 |
Exac | rs727502787 |
Gnomad | rs727502787 |
Varsome | rs727502787 |
LitVar | rs727502787 |
Map | rs727502787 |
PheGenI | rs727502787 |
Biobank | rs727502787 |
1000 genomes | rs727502787 |
hgdp | rs727502787 |
ensembl | rs727502787 |
geneview | rs727502787 |
scholar | rs727502787 |
rs727502787 | |
pharmgkb | rs727502787 |
gwascentral | rs727502787 |
openSNP | rs727502787 |
23andMe | rs727502787 |
SNPshot | rs727502787 |
SNPdbe | rs727502787 |
MSV3d | rs727502787 |
GWAS Ctlg | rs727502787 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs727502787(G;G) |
Alt | rs727502787(G;G) |
Reference | Rs727502787(A;A) |
Significance | Pathogenic |
Disease | Common variable immunodeficiency 10 |
Variation | info |
Gene | PSD NFKB2 |
CLNDBN | Common variable immunodeficiency 10 |
Reversed | 0 |
HGVS | NC_000010.10:g.104162024A>G |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000150032.3, |