rs796052961
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs796052961(C;C) |
Make rs796052961(C;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 2 |
Position | 166052884 |
Gene | SCN1A |
is a | snp |
is | mentioned by |
dbSNP | rs796052961 |
dbSNP (classic) | rs796052961 |
ClinGen | rs796052961 |
ebi | rs796052961 |
HLI | rs796052961 |
Exac | rs796052961 |
Gnomad | rs796052961 |
Varsome | rs796052961 |
LitVar | rs796052961 |
Map | rs796052961 |
PheGenI | rs796052961 |
Biobank | rs796052961 |
1000 genomes | rs796052961 |
hgdp | rs796052961 |
ensembl | rs796052961 |
geneview | rs796052961 |
scholar | rs796052961 |
rs796052961 | |
pharmgkb | rs796052961 |
gwascentral | rs796052961 |
openSNP | rs796052961 |
23andMe | rs796052961 |
SNPshot | rs796052961 |
SNPdbe | rs796052961 |
MSV3d | rs796052961 |
GWAS Ctlg | rs796052961 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs796052961(C;C) |
Alt | rs796052961(C;C) |
Reference | Rs796052961(T;T) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | SCN1A |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000002.11:g.166909394A>G |
CLNSRC | |
CLNACC | RCV000188840.2, |