rs797045143
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs797045143(C;T) |
Make rs797045143(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 19 |
Position | 2438464 |
Gene | LMNB2 |
is a | snp |
is | mentioned by |
dbSNP | rs797045143 |
dbSNP (classic) | rs797045143 |
ClinGen | rs797045143 |
ebi | rs797045143 |
HLI | rs797045143 |
Exac | rs797045143 |
Gnomad | rs797045143 |
Varsome | rs797045143 |
LitVar | rs797045143 |
Map | rs797045143 |
PheGenI | rs797045143 |
Biobank | rs797045143 |
1000 genomes | rs797045143 |
hgdp | rs797045143 |
ensembl | rs797045143 |
geneview | rs797045143 |
scholar | rs797045143 |
rs797045143 | |
pharmgkb | rs797045143 |
gwascentral | rs797045143 |
openSNP | rs797045143 |
23andMe | rs797045143 |
SNPshot | rs797045143 |
SNPdbe | rs797045143 |
MSV3d | rs797045143 |
GWAS Ctlg | rs797045143 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs797045143(T;T) |
Alt | rs797045143(T;T) |
Reference | Rs797045143(C;C) |
Significance | Pathogenic |
Disease | Epilepsy |
Variation | info |
Gene | LMNB2 |
CLNDBN | Epilepsy, progressive myoclonic, 9 |
Reversed | 1 |
HGVS | NC_000019.9:g.2438462G>A |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000190899.2, |