rs1064793263
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Chromosome | 12 |
Position | 51790404 |
Gene | SCN8A |
is a | snp |
is | mentioned by |
dbSNP | rs1064793263 |
dbSNP (classic) | rs1064793263 |
ClinGen | rs1064793263 |
ebi | rs1064793263 |
HLI | rs1064793263 |
Exac | rs1064793263 |
Gnomad | rs1064793263 |
Varsome | rs1064793263 |
LitVar | rs1064793263 |
Map | rs1064793263 |
PheGenI | rs1064793263 |
Biobank | rs1064793263 |
1000 genomes | rs1064793263 |
hgdp | rs1064793263 |
ensembl | rs1064793263 |
geneview | rs1064793263 |
scholar | rs1064793263 |
rs1064793263 | |
pharmgkb | rs1064793263 |
gwascentral | rs1064793263 |
openSNP | rs1064793263 |
23andMe | rs1064793263 |
SNPshot | rs1064793263 |
SNPdbe | rs1064793263 |
MSV3d | rs1064793263 |
GWAS Ctlg | rs1064793263 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1064793263(A;A) |
Alt | rs1064793263(A;A) |
Reference | Rs1064793263(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | SCN8A |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000012.11:g.52184188G>A |
CLNSRC | |
CLNACC | RCV000480970.1, |