rs28937874
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs28937874(A;C) |
Make rs28937874(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 10 |
Position | 93797277 |
Gene | LGI1 |
is a | snp |
is | mentioned by |
dbSNP | rs28937874 |
dbSNP (classic) | rs28937874 |
ClinGen | rs28937874 |
ebi | rs28937874 |
HLI | rs28937874 |
Exac | rs28937874 |
Gnomad | rs28937874 |
Varsome | rs28937874 |
LitVar | rs28937874 |
Map | rs28937874 |
PheGenI | rs28937874 |
Biobank | rs28937874 |
1000 genomes | rs28937874 |
hgdp | rs28937874 |
ensembl | rs28937874 |
geneview | rs28937874 |
scholar | rs28937874 |
rs28937874 | |
pharmgkb | rs28937874 |
gwascentral | rs28937874 |
openSNP | rs28937874 |
23andMe | rs28937874 |
SNPshot | rs28937874 |
SNPdbe | rs28937874 |
MSV3d | rs28937874 |
GWAS Ctlg | rs28937874 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs28937874(C;C) |
Alt | rs28937874(C;C) |
Reference | Rs28937874(A;A) |
Significance | Pathogenic |
Disease | Epilepsy |
Variation | info |
Gene | LGI1 |
CLNDBN | Epilepsy, lateral temporal lobe, autosomal dominant |
Reversed | 0 |
HGVS | NC_000010.10:g.95557034A>C |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000005763.2, |