rs770501034
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs770501034(C;T) |
Make rs770501034(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 8 |
Position | 74364059 |
Gene | GDAP1 |
is a | snp |
is | mentioned by |
dbSNP | rs770501034 |
dbSNP (classic) | rs770501034 |
ClinGen | rs770501034 |
ebi | rs770501034 |
HLI | rs770501034 |
Exac | rs770501034 |
Gnomad | rs770501034 |
Varsome | rs770501034 |
LitVar | rs770501034 |
Map | rs770501034 |
PheGenI | rs770501034 |
Biobank | rs770501034 |
1000 genomes | rs770501034 |
hgdp | rs770501034 |
ensembl | rs770501034 |
geneview | rs770501034 |
scholar | rs770501034 |
rs770501034 | |
pharmgkb | rs770501034 |
gwascentral | rs770501034 |
openSNP | rs770501034 |
23andMe | rs770501034 |
SNPshot | rs770501034 |
SNPdbe | rs770501034 |
MSV3d | rs770501034 |
GWAS Ctlg | rs770501034 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs770501034(T;T) |
Alt | rs770501034(T;T) |
Reference | Rs770501034(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | GDAP1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000008.10:g.75276294C>T |
CLNSRC | |
CLNACC | RCV000235362.1, |