rs772909106
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs772909106(A;A) |
Make rs772909106(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 1 |
Position | 236754026 |
Gene | ACTN2 |
is a | snp |
is | mentioned by |
dbSNP | rs772909106 |
dbSNP (classic) | rs772909106 |
ClinGen | rs772909106 |
ebi | rs772909106 |
HLI | rs772909106 |
Exac | rs772909106 |
Gnomad | rs772909106 |
Varsome | rs772909106 |
LitVar | rs772909106 |
Map | rs772909106 |
PheGenI | rs772909106 |
Biobank | rs772909106 |
1000 genomes | rs772909106 |
hgdp | rs772909106 |
ensembl | rs772909106 |
geneview | rs772909106 |
scholar | rs772909106 |
rs772909106 | |
pharmgkb | rs772909106 |
gwascentral | rs772909106 |
openSNP | rs772909106 |
23andMe | rs772909106 |
SNPshot | rs772909106 |
SNPdbe | rs772909106 |
MSV3d | rs772909106 |
GWAS Ctlg | rs772909106 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs772909106(A;A) |
Alt | rs772909106(A;A) |
Reference | Rs772909106(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | ACTN2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.236917326G>A |
CLNSRC | |
CLNACC | RCV000183267.2, |