rs869312914
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs869312914(C;T) |
Make rs869312914(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 14 |
Position | 67752520 |
Gene | ZFYVE26 |
is a | snp |
is | mentioned by |
dbSNP | rs869312914 |
dbSNP (classic) | rs869312914 |
ClinGen | rs869312914 |
ebi | rs869312914 |
HLI | rs869312914 |
Exac | rs869312914 |
Gnomad | rs869312914 |
Varsome | rs869312914 |
LitVar | rs869312914 |
Map | rs869312914 |
PheGenI | rs869312914 |
Biobank | rs869312914 |
1000 genomes | rs869312914 |
hgdp | rs869312914 |
ensembl | rs869312914 |
geneview | rs869312914 |
scholar | rs869312914 |
rs869312914 | |
pharmgkb | rs869312914 |
gwascentral | rs869312914 |
openSNP | rs869312914 |
23andMe | rs869312914 |
SNPshot | rs869312914 |
SNPdbe | rs869312914 |
MSV3d | rs869312914 |
GWAS Ctlg | rs869312914 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs869312914(T;T) |
Alt | rs869312914(T;T) |
Reference | Rs869312914(C;C) |
Significance | Pathogenic |
Disease | Inborn genetic diseases |
Variation | info |
Gene | ZFYVE26 |
CLNDBN | Inborn genetic diseases |
Reversed | 1 |
HGVS | NC_000014.8:g.68219237G>A |
CLNSRC | |
CLNACC | RCV000210660.1, |