rs786205724
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs786205724(C;T) |
Make rs786205724(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 4 |
Position | 113282730 |
Gene | ANK2 |
is a | snp |
is | mentioned by |
dbSNP | rs786205724 |
dbSNP (classic) | rs786205724 |
ClinGen | rs786205724 |
ebi | rs786205724 |
HLI | rs786205724 |
Exac | rs786205724 |
Gnomad | rs786205724 |
Varsome | rs786205724 |
LitVar | rs786205724 |
Map | rs786205724 |
PheGenI | rs786205724 |
Biobank | rs786205724 |
1000 genomes | rs786205724 |
hgdp | rs786205724 |
ensembl | rs786205724 |
geneview | rs786205724 |
scholar | rs786205724 |
rs786205724 | |
pharmgkb | rs786205724 |
gwascentral | rs786205724 |
openSNP | rs786205724 |
23andMe | rs786205724 |
SNPshot | rs786205724 |
SNPdbe | rs786205724 |
MSV3d | rs786205724 |
GWAS Ctlg | rs786205724 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs786205724(T;T) |
Alt | rs786205724(T;T) |
Reference | Rs786205724(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | ANK2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000004.11:g.114203886C>T |
CLNSRC | |
CLNACC | RCV000170682.5, |