rs752283089
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs752283089(G;T) |
Make rs752283089(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 14 |
Position | 67783217 |
Gene | ZFYVE26 |
is a | snp |
is | mentioned by |
dbSNP | rs752283089 |
dbSNP (classic) | rs752283089 |
ClinGen | rs752283089 |
ebi | rs752283089 |
HLI | rs752283089 |
Exac | rs752283089 |
Gnomad | rs752283089 |
Varsome | rs752283089 |
LitVar | rs752283089 |
Map | rs752283089 |
PheGenI | rs752283089 |
Biobank | rs752283089 |
1000 genomes | rs752283089 |
hgdp | rs752283089 |
ensembl | rs752283089 |
geneview | rs752283089 |
scholar | rs752283089 |
rs752283089 | |
pharmgkb | rs752283089 |
gwascentral | rs752283089 |
openSNP | rs752283089 |
23andMe | rs752283089 |
SNPshot | rs752283089 |
SNPdbe | rs752283089 |
MSV3d | rs752283089 |
GWAS Ctlg | rs752283089 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs752283089(T;T) |
Alt | rs752283089(T;T) |
Reference | Rs752283089(G;G) |
Significance | Pathogenic |
Disease | Inborn genetic diseases |
Variation | info |
Gene | ZFYVE26 |
CLNDBN | Inborn genetic diseases |
Reversed | 0 |
HGVS | NC_000014.8:g.68249934G>T |
CLNSRC | |
CLNACC | RCV000210539.1, |