rs2296949
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
(G;G) | 0 |
Make rs2296949(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 131510049 |
Gene | POMT1 |
is a | snp |
is | mentioned by |
dbSNP | rs2296949 |
dbSNP (classic) | rs2296949 |
ClinGen | rs2296949 |
ebi | rs2296949 |
HLI | rs2296949 |
Exac | rs2296949 |
Gnomad | rs2296949 |
Varsome | rs2296949 |
LitVar | rs2296949 |
Map | rs2296949 |
PheGenI | rs2296949 |
Biobank | rs2296949 |
1000 genomes | rs2296949 |
hgdp | rs2296949 |
ensembl | rs2296949 |
geneview | rs2296949 |
scholar | rs2296949 |
rs2296949 | |
pharmgkb | rs2296949 |
gwascentral | rs2296949 |
openSNP | rs2296949 |
23andMe | rs2296949 |
SNPshot | rs2296949 |
SNPdbe | rs2296949 |
MSV3d | rs2296949 |
GWAS Ctlg | rs2296949 |
GMAF | 0.1341 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
ClinVar | |
---|---|
Risk | Rs2296949(G;G) |
Alt | Rs2296949(G;G) |
Reference | Rs2296949(A;A) |
Significance | Non-pathogenic |
Disease | not specified |
Variation | info |
Gene | POMT1 |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000009.11:g.134385436A\x3d; NC_000009.11:g.134385436A>G |
CLNSRC | ClinVar Emory University |
CLNACC | RCV000081493.5, RCV000216907.1, |