rs398124226
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs398124226(A;A) |
Make rs398124226(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 20 |
Position | 18525021 |
Gene | SEC23B |
is a | snp |
is | mentioned by |
dbSNP | rs398124226 |
dbSNP (classic) | rs398124226 |
ClinGen | rs398124226 |
ebi | rs398124226 |
HLI | rs398124226 |
Exac | rs398124226 |
Gnomad | rs398124226 |
Varsome | rs398124226 |
LitVar | rs398124226 |
Map | rs398124226 |
PheGenI | rs398124226 |
Biobank | rs398124226 |
1000 genomes | rs398124226 |
hgdp | rs398124226 |
ensembl | rs398124226 |
geneview | rs398124226 |
scholar | rs398124226 |
rs398124226 | |
pharmgkb | rs398124226 |
gwascentral | rs398124226 |
openSNP | rs398124226 |
23andMe | rs398124226 |
SNPshot | rs398124226 |
SNPdbe | rs398124226 |
MSV3d | rs398124226 |
GWAS Ctlg | rs398124226 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs398124226(A;A) rs398124226(C;C) |
Alt | rs398124226(A;A) rs398124226(C;C) |
Reference | Rs398124226(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | SEC23B |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000020.10:g.18505665G>A |
CLNSRC | HGMD |
CLNACC | RCV000081409.4, |