rs1064794243
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Chromosome | 17 |
Position | 63941169 |
Gene | SCN4A |
is a | snp |
is | mentioned by |
dbSNP | rs1064794243 |
dbSNP (classic) | rs1064794243 |
ClinGen | rs1064794243 |
ebi | rs1064794243 |
HLI | rs1064794243 |
Exac | rs1064794243 |
Gnomad | rs1064794243 |
Varsome | rs1064794243 |
LitVar | rs1064794243 |
Map | rs1064794243 |
PheGenI | rs1064794243 |
Biobank | rs1064794243 |
1000 genomes | rs1064794243 |
hgdp | rs1064794243 |
ensembl | rs1064794243 |
geneview | rs1064794243 |
scholar | rs1064794243 |
rs1064794243 | |
pharmgkb | rs1064794243 |
gwascentral | rs1064794243 |
openSNP | rs1064794243 |
23andMe | rs1064794243 |
SNPshot | rs1064794243 |
SNPdbe | rs1064794243 |
MSV3d | rs1064794243 |
GWAS Ctlg | rs1064794243 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1064794243(A;A) |
Alt | rs1064794243(A;A) |
Reference | Rs1064794243(T;T) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | SCN4A |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000017.10:g.62018529A>T |
CLNSRC | |
CLNACC | RCV000484046.1, |