rs796053222
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs796053222(C;C) |
Make rs796053222(C;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 12 |
Position | 51806375 |
Gene | SCN8A |
is a | snp |
is | mentioned by |
dbSNP | rs796053222 |
dbSNP (classic) | rs796053222 |
ClinGen | rs796053222 |
ebi | rs796053222 |
HLI | rs796053222 |
Exac | rs796053222 |
Gnomad | rs796053222 |
Varsome | rs796053222 |
LitVar | rs796053222 |
Map | rs796053222 |
PheGenI | rs796053222 |
Biobank | rs796053222 |
1000 genomes | rs796053222 |
hgdp | rs796053222 |
ensembl | rs796053222 |
geneview | rs796053222 |
scholar | rs796053222 |
rs796053222 | |
pharmgkb | rs796053222 |
gwascentral | rs796053222 |
openSNP | rs796053222 |
23andMe | rs796053222 |
SNPshot | rs796053222 |
SNPdbe | rs796053222 |
MSV3d | rs796053222 |
GWAS Ctlg | rs796053222 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs796053222(C;C) |
Alt | rs796053222(C;C) |
Reference | Rs796053222(T;T) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | SCN8A |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000012.11:g.52200159T>C |
CLNSRC | |
CLNACC | RCV000189283.1, |