rs28937594
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 6 | Inclusion Body Myopathy, type 2 |
(C;T) | 3 | Carrier of one inclusion body myopathy mutation |
(T;T) | 0 | common in clinvar |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 36217399 |
Gene | GNE |
is a | snp |
is | mentioned by |
dbSNP | rs28937594 |
dbSNP (classic) | rs28937594 |
ClinGen | rs28937594 |
ebi | rs28937594 |
HLI | rs28937594 |
Exac | rs28937594 |
Gnomad | rs28937594 |
Varsome | rs28937594 |
LitVar | rs28937594 |
Map | rs28937594 |
PheGenI | rs28937594 |
Biobank | rs28937594 |
1000 genomes | rs28937594 |
hgdp | rs28937594 |
ensembl | rs28937594 |
geneview | rs28937594 |
scholar | rs28937594 |
rs28937594 | |
pharmgkb | rs28937594 |
gwascentral | rs28937594 |
openSNP | rs28937594 |
23andMe | rs28937594 |
SNPshot | rs28937594 |
SNPdbe | rs28937594 |
MSV3d | rs28937594 |
GWAS Ctlg | rs28937594 |
Max Magnitude | 6 |
rs28937594, also known as c.2228T>C, p.Met743Thr, M743T and most commonly in the literature M712T, is a mutation in the GNE gene on chromosome 9.
The very rare rs28937594(C) allele is the most common mutation leading to autosomal recessive inclusion body myopathy 2 (IBM2 or HIBM) in Middle Eastern populations.[PMID 12743242]
See also OMIM 603824.0005
ClinVar | |
---|---|
Risk | Rs28937594(C;C) |
Alt | Rs28937594(C;C) |
Reference | Rs28937594(T;T) |
Significance | Pathogenic |
Disease | Inclusion body myopathy 2 Nonaka myopathy Sialuria not provided |
Variation | info |
Gene | GNE |
CLNDBN | Inclusion body myopathy 2 Nonaka myopathy Sialuria not provided |
Reversed | 1 |
HGVS | NC_000009.11:g.36217396A>G |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000006395.9, RCV000006396.4, RCV000350827.1, RCV000443895.1, |