rs752704424
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs752704424(A;A) |
Make rs752704424(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 4 |
Position | 113355873 |
Gene | ANK2 |
is a | snp |
is | mentioned by |
dbSNP | rs752704424 |
dbSNP (classic) | rs752704424 |
ClinGen | rs752704424 |
ebi | rs752704424 |
HLI | rs752704424 |
Exac | rs752704424 |
Gnomad | rs752704424 |
Varsome | rs752704424 |
LitVar | rs752704424 |
Map | rs752704424 |
PheGenI | rs752704424 |
Biobank | rs752704424 |
1000 genomes | rs752704424 |
hgdp | rs752704424 |
ensembl | rs752704424 |
geneview | rs752704424 |
scholar | rs752704424 |
rs752704424 | |
pharmgkb | rs752704424 |
gwascentral | rs752704424 |
openSNP | rs752704424 |
23andMe | rs752704424 |
SNPshot | rs752704424 |
SNPdbe | rs752704424 |
MSV3d | rs752704424 |
GWAS Ctlg | rs752704424 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs752704424(A;A) |
Alt | rs752704424(A;A) |
Reference | Rs752704424(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided not specified |
Variation | info |
Gene | ANK2 |
CLNDBN | not provided not specified |
Reversed | 0 |
HGVS | NC_000004.11:g.114277029G>A |
CLNSRC | |
CLNACC | RCV000171379.1, RCV000480336.1, |