rs796053198
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs796053198(-;-) |
Make rs796053198(-;C) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 2 |
Position | 165310333 |
Gene | SCN2A |
is a | snp |
is | mentioned by |
dbSNP | rs796053198 |
dbSNP (classic) | rs796053198 |
ClinGen | rs796053198 |
ebi | rs796053198 |
HLI | rs796053198 |
Exac | rs796053198 |
Gnomad | rs796053198 |
Varsome | rs796053198 |
LitVar | rs796053198 |
Map | rs796053198 |
PheGenI | rs796053198 |
Biobank | rs796053198 |
1000 genomes | rs796053198 |
hgdp | rs796053198 |
ensembl | rs796053198 |
geneview | rs796053198 |
scholar | rs796053198 |
rs796053198 | |
pharmgkb | rs796053198 |
gwascentral | rs796053198 |
openSNP | rs796053198 |
23andMe | rs796053198 |
SNPshot | rs796053198 |
SNPdbe | rs796053198 |
MSV3d | rs796053198 |
GWAS Ctlg | rs796053198 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs796053198(-;-) |
Alt | rs796053198(-;-) |
Reference | Rs796053198(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | SCN2A |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.166166843delC |
CLNSRC | |
CLNACC | RCV000189236.1, |