rs534934297
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs534934297(A;G) |
Make rs534934297(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 4 |
Position | 113356942 |
Gene | ANK2 |
is a | snp |
is | mentioned by |
dbSNP | rs534934297 |
dbSNP (classic) | rs534934297 |
ClinGen | rs534934297 |
ebi | rs534934297 |
HLI | rs534934297 |
Exac | rs534934297 |
Gnomad | rs534934297 |
Varsome | rs534934297 |
LitVar | rs534934297 |
Map | rs534934297 |
PheGenI | rs534934297 |
Biobank | rs534934297 |
1000 genomes | rs534934297 |
hgdp | rs534934297 |
ensembl | rs534934297 |
geneview | rs534934297 |
scholar | rs534934297 |
rs534934297 | |
pharmgkb | rs534934297 |
gwascentral | rs534934297 |
openSNP | rs534934297 |
23andMe | rs534934297 |
SNPshot | rs534934297 |
SNPdbe | rs534934297 |
MSV3d | rs534934297 |
GWAS Ctlg | rs534934297 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs534934297(G;G) |
Alt | rs534934297(G;G) |
Reference | Rs534934297(A;A) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | ANK2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000004.11:g.114278098A>G |
CLNSRC | |
CLNACC | RCV000171381.1, |