rs756121249
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs756121249(A;A) |
Make rs756121249(A;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 8 |
Position | 74350570 |
Gene | GDAP1 |
is a | snp |
is | mentioned by |
dbSNP | rs756121249 |
dbSNP (classic) | rs756121249 |
ClinGen | rs756121249 |
ebi | rs756121249 |
HLI | rs756121249 |
Exac | rs756121249 |
Gnomad | rs756121249 |
Varsome | rs756121249 |
LitVar | rs756121249 |
Map | rs756121249 |
PheGenI | rs756121249 |
Biobank | rs756121249 |
1000 genomes | rs756121249 |
hgdp | rs756121249 |
ensembl | rs756121249 |
geneview | rs756121249 |
scholar | rs756121249 |
rs756121249 | |
pharmgkb | rs756121249 |
gwascentral | rs756121249 |
openSNP | rs756121249 |
23andMe | rs756121249 |
SNPshot | rs756121249 |
SNPdbe | rs756121249 |
MSV3d | rs756121249 |
GWAS Ctlg | rs756121249 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs756121249(A;A) |
Alt | rs756121249(A;A) |
Reference | Rs756121249(T;T) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | GDAP1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000008.10:g.75262805T>A |
CLNSRC | |
CLNACC | RCV000489068.1, |