rs896431562
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 8 |
Position | 74350550 |
Gene | GDAP1 |
is a | snp |
is | mentioned by |
dbSNP | rs896431562 |
dbSNP (classic) | rs896431562 |
ClinGen | rs896431562 |
ebi | rs896431562 |
HLI | rs896431562 |
Exac | rs896431562 |
Gnomad | rs896431562 |
Varsome | rs896431562 |
LitVar | rs896431562 |
Map | rs896431562 |
PheGenI | rs896431562 |
Biobank | rs896431562 |
1000 genomes | rs896431562 |
hgdp | rs896431562 |
ensembl | rs896431562 |
geneview | rs896431562 |
scholar | rs896431562 |
rs896431562 | |
pharmgkb | rs896431562 |
gwascentral | rs896431562 |
openSNP | rs896431562 |
23andMe | rs896431562 |
SNPshot | rs896431562 |
SNPdbe | rs896431562 |
MSV3d | rs896431562 |
GWAS Ctlg | rs896431562 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs896431562(T;T) |
Alt | rs896431562(T;T) |
Reference | Rs896431562(A;A) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | GDAP1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000008.10:g.75262785A>T |
CLNSRC | |
CLNACC | RCV000482807.1, |