rs139425890
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs139425890(A;A) |
Make rs139425890(A;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 36246120 |
Gene | GNE |
is a | snp |
is | mentioned by |
dbSNP | rs139425890 |
dbSNP (classic) | rs139425890 |
ClinGen | rs139425890 |
ebi | rs139425890 |
HLI | rs139425890 |
Exac | rs139425890 |
Gnomad | rs139425890 |
Varsome | rs139425890 |
LitVar | rs139425890 |
Map | rs139425890 |
PheGenI | rs139425890 |
Biobank | rs139425890 |
1000 genomes | rs139425890 |
hgdp | rs139425890 |
ensembl | rs139425890 |
geneview | rs139425890 |
scholar | rs139425890 |
rs139425890 | |
pharmgkb | rs139425890 |
gwascentral | rs139425890 |
openSNP | rs139425890 |
23andMe | rs139425890 |
SNPshot | rs139425890 |
SNPdbe | rs139425890 |
MSV3d | rs139425890 |
GWAS Ctlg | rs139425890 |
GMAF | 0.0009183 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs139425890(A;A) |
Alt | rs139425890(A;A) |
Reference | Rs139425890(T;T) |
Significance | Other |
Disease | Inclusion body myopathy 2 Nonaka myopathy |
Variation | info |
Gene | GNE |
CLNDBN | Inclusion body myopathy 2 Nonaka myopathy |
Reversed | 0 |
HGVS | NC_000009.11:g.36246117T>A |
CLNSRC | UniProtKB (protein) |
CLNACC | RCV000034132.3, RCV000343796.1, |