rs768176054
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs768176054(-;-) |
Make rs768176054(-;A) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 14 |
Position | 67793711 |
Gene | ZFYVE26 |
is a | snp |
is | mentioned by |
dbSNP | rs768176054 |
dbSNP (classic) | rs768176054 |
ClinGen | rs768176054 |
ebi | rs768176054 |
HLI | rs768176054 |
Exac | rs768176054 |
Gnomad | rs768176054 |
Varsome | rs768176054 |
LitVar | rs768176054 |
Map | rs768176054 |
PheGenI | rs768176054 |
Biobank | rs768176054 |
1000 genomes | rs768176054 |
hgdp | rs768176054 |
ensembl | rs768176054 |
geneview | rs768176054 |
scholar | rs768176054 |
rs768176054 | |
pharmgkb | rs768176054 |
gwascentral | rs768176054 |
openSNP | rs768176054 |
23andMe | rs768176054 |
SNPshot | rs768176054 |
SNPdbe | rs768176054 |
MSV3d | rs768176054 |
GWAS Ctlg | rs768176054 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs768176054(-;-) |
Alt | rs768176054(-;-) |
Reference | Rs768176054(A;A) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ZFYVE26 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000014.8:g.68260428delA |
CLNSRC | |
CLNACC | RCV000494368.1, |