rs775709247
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs775709247(C;C) |
Make rs775709247(C;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 14 |
Position | 67802285 |
Gene | ZFYVE26 |
is a | snp |
is | mentioned by |
dbSNP | rs775709247 |
dbSNP (classic) | rs775709247 |
ClinGen | rs775709247 |
ebi | rs775709247 |
HLI | rs775709247 |
Exac | rs775709247 |
Gnomad | rs775709247 |
Varsome | rs775709247 |
LitVar | rs775709247 |
Map | rs775709247 |
PheGenI | rs775709247 |
Biobank | rs775709247 |
1000 genomes | rs775709247 |
hgdp | rs775709247 |
ensembl | rs775709247 |
geneview | rs775709247 |
scholar | rs775709247 |
rs775709247 | |
pharmgkb | rs775709247 |
gwascentral | rs775709247 |
openSNP | rs775709247 |
23andMe | rs775709247 |
SNPshot | rs775709247 |
SNPdbe | rs775709247 |
MSV3d | rs775709247 |
GWAS Ctlg | rs775709247 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs775709247(C;C) |
Alt | rs775709247(C;C) |
Reference | Rs775709247(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | ZFYVE26 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000014.8:g.68269002G>C |
CLNSRC | |
CLNACC | RCV000493196.1, |