rs1064795159
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Chromosome | 2 |
Position | 165314029 |
Gene | SCN2A |
is a | snp |
is | mentioned by |
dbSNP | rs1064795159 |
dbSNP (classic) | rs1064795159 |
ClinGen | rs1064795159 |
ebi | rs1064795159 |
HLI | rs1064795159 |
Exac | rs1064795159 |
Gnomad | rs1064795159 |
Varsome | rs1064795159 |
LitVar | rs1064795159 |
Map | rs1064795159 |
PheGenI | rs1064795159 |
Biobank | rs1064795159 |
1000 genomes | rs1064795159 |
hgdp | rs1064795159 |
ensembl | rs1064795159 |
geneview | rs1064795159 |
scholar | rs1064795159 |
rs1064795159 | |
pharmgkb | rs1064795159 |
gwascentral | rs1064795159 |
openSNP | rs1064795159 |
23andMe | rs1064795159 |
SNPshot | rs1064795159 |
SNPdbe | rs1064795159 |
MSV3d | rs1064795159 |
GWAS Ctlg | rs1064795159 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1064795159(T;T) |
Alt | rs1064795159(T;T) |
Reference | Rs1064795159(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | SCN2A |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.166170539C>T |
CLNSRC | |
CLNACC | RCV000478420.1, |