rs1064795711
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Chromosome | 3 |
Position | 38903990 |
Gene | SCN11A |
is a | snp |
is | mentioned by |
dbSNP | rs1064795711 |
dbSNP (classic) | rs1064795711 |
ClinGen | rs1064795711 |
ebi | rs1064795711 |
HLI | rs1064795711 |
Exac | rs1064795711 |
Gnomad | rs1064795711 |
Varsome | rs1064795711 |
LitVar | rs1064795711 |
Map | rs1064795711 |
PheGenI | rs1064795711 |
Biobank | rs1064795711 |
1000 genomes | rs1064795711 |
hgdp | rs1064795711 |
ensembl | rs1064795711 |
geneview | rs1064795711 |
scholar | rs1064795711 |
rs1064795711 | |
pharmgkb | rs1064795711 |
gwascentral | rs1064795711 |
openSNP | rs1064795711 |
23andMe | rs1064795711 |
SNPshot | rs1064795711 |
SNPdbe | rs1064795711 |
MSV3d | rs1064795711 |
GWAS Ctlg | rs1064795711 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1064795711(A;A) |
Alt | rs1064795711(A;A) |
Reference | Rs1064795711(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | SCN11A |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000003.11:g.38945481C>T |
CLNSRC | |
CLNACC | RCV000480155.1, |