rs36023150
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs36023150(G;T) |
Make rs36023150(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 20 |
Position | 18524556 |
Gene | SEC23B |
is a | snp |
is | mentioned by |
dbSNP | rs36023150 |
dbSNP (classic) | rs36023150 |
ClinGen | rs36023150 |
ebi | rs36023150 |
HLI | rs36023150 |
Exac | rs36023150 |
Gnomad | rs36023150 |
Varsome | rs36023150 |
LitVar | rs36023150 |
Map | rs36023150 |
PheGenI | rs36023150 |
Biobank | rs36023150 |
1000 genomes | rs36023150 |
hgdp | rs36023150 |
ensembl | rs36023150 |
geneview | rs36023150 |
scholar | rs36023150 |
rs36023150 | |
pharmgkb | rs36023150 |
gwascentral | rs36023150 |
openSNP | rs36023150 |
23andMe | rs36023150 |
SNPshot | rs36023150 |
SNPdbe | rs36023150 |
MSV3d | rs36023150 |
GWAS Ctlg | rs36023150 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs36023150(T;T) |
Alt | rs36023150(T;T) |
Reference | Rs36023150(G;G) |
Significance | Pathogenic |
Disease | not specified Cowden syndrome 7 Congenital dyserythropoietic anemia |
Variation | info |
Gene | SEC23B |
CLNDBN | not specified Cowden syndrome 7 Congenital dyserythropoietic anemia |
Reversed | 0 |
HGVS | NC_000020.10:g.18505200G>T |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000081408.4, RCV000210063.1, RCV000269836.1, |