rs368287711
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs368287711(A;A) |
Make rs368287711(A;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 117989554 |
Gene | IL10RA |
is a | snp |
is | mentioned by |
dbSNP | rs368287711 |
dbSNP (classic) | rs368287711 |
ClinGen | rs368287711 |
ebi | rs368287711 |
HLI | rs368287711 |
Exac | rs368287711 |
Gnomad | rs368287711 |
Varsome | rs368287711 |
LitVar | rs368287711 |
Map | rs368287711 |
PheGenI | rs368287711 |
Biobank | rs368287711 |
1000 genomes | rs368287711 |
hgdp | rs368287711 |
ensembl | rs368287711 |
geneview | rs368287711 |
scholar | rs368287711 |
rs368287711 | |
pharmgkb | rs368287711 |
gwascentral | rs368287711 |
openSNP | rs368287711 |
23andMe | rs368287711 |
SNPshot | rs368287711 |
SNPdbe | rs368287711 |
MSV3d | rs368287711 |
GWAS Ctlg | rs368287711 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs368287711(A;A) rs368287711(T;T) |
Alt | rs368287711(A;A) rs368287711(T;T) |
Reference | Rs368287711(C;C) |
Significance | Pathogenic |
Disease | Inflammatory bowel disease 28 |
Variation | info |
Gene | IL10RA |
CLNDBN | Inflammatory bowel disease 28 |
Reversed | 0 |
HGVS | NC_000011.9:g.117860269C>T |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000032627.26, |