rs529961953
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs529961953(A;A) |
Make rs529961953(A;C) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 11 |
Position | 22257738 |
Gene | ANO5 |
is a | snp |
is | mentioned by |
dbSNP | rs529961953 |
dbSNP (classic) | rs529961953 |
ClinGen | rs529961953 |
ebi | rs529961953 |
HLI | rs529961953 |
Exac | rs529961953 |
Gnomad | rs529961953 |
Varsome | rs529961953 |
LitVar | rs529961953 |
Map | rs529961953 |
PheGenI | rs529961953 |
Biobank | rs529961953 |
1000 genomes | rs529961953 |
hgdp | rs529961953 |
ensembl | rs529961953 |
geneview | rs529961953 |
scholar | rs529961953 |
rs529961953 | |
pharmgkb | rs529961953 |
gwascentral | rs529961953 |
openSNP | rs529961953 |
23andMe | rs529961953 |
SNPshot | rs529961953 |
SNPdbe | rs529961953 |
MSV3d | rs529961953 |
GWAS Ctlg | rs529961953 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs529961953(A;A) |
Alt | rs529961953(A;A) |
Reference | Rs529961953(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ANO5 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000011.9:g.22279284C>A |
CLNSRC | |
CLNACC | RCV000438945.1, |