rs770694933
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs770694933(-;-) |
Make rs770694933(-;C) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 11 |
Position | 22276149 |
Gene | ANO5 |
is a | snp |
is | mentioned by |
dbSNP | rs770694933 |
dbSNP (classic) | rs770694933 |
ClinGen | rs770694933 |
ebi | rs770694933 |
HLI | rs770694933 |
Exac | rs770694933 |
Gnomad | rs770694933 |
Varsome | rs770694933 |
LitVar | rs770694933 |
Map | rs770694933 |
PheGenI | rs770694933 |
Biobank | rs770694933 |
1000 genomes | rs770694933 |
hgdp | rs770694933 |
ensembl | rs770694933 |
geneview | rs770694933 |
scholar | rs770694933 |
rs770694933 | |
pharmgkb | rs770694933 |
gwascentral | rs770694933 |
openSNP | rs770694933 |
23andMe | rs770694933 |
SNPshot | rs770694933 |
SNPdbe | rs770694933 |
MSV3d | rs770694933 |
GWAS Ctlg | rs770694933 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | |
Alt | |
Reference | Rs770694933(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ANO5 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000011.9:g.22297695delC |
CLNSRC | |
CLNACC | RCV000313812.1, |