rs769520392
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs769520392(A;G) |
Make rs769520392(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 12 |
Position | 51706525 |
Gene | SCN8A |
is a | snp |
is | mentioned by |
dbSNP | rs769520392 |
dbSNP (classic) | rs769520392 |
ClinGen | rs769520392 |
ebi | rs769520392 |
HLI | rs769520392 |
Exac | rs769520392 |
Gnomad | rs769520392 |
Varsome | rs769520392 |
LitVar | rs769520392 |
Map | rs769520392 |
PheGenI | rs769520392 |
Biobank | rs769520392 |
1000 genomes | rs769520392 |
hgdp | rs769520392 |
ensembl | rs769520392 |
geneview | rs769520392 |
scholar | rs769520392 |
rs769520392 | |
pharmgkb | rs769520392 |
gwascentral | rs769520392 |
openSNP | rs769520392 |
23andMe | rs769520392 |
SNPshot | rs769520392 |
SNPdbe | rs769520392 |
MSV3d | rs769520392 |
GWAS Ctlg | rs769520392 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs769520392(G;G) |
Alt | rs769520392(G;G) |
Reference | Rs769520392(A;A) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | SCN8A |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000012.11:g.52100309A>G |
CLNSRC | |
CLNACC | RCV000434079.1, |