rs28933402
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | |
(G;G) | 0 | common in clinvar |
Make rs28933402(A;A) |
Make rs28933402(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 133353893 |
Gene | SURF1 |
is a | snp |
is | mentioned by |
dbSNP | rs28933402 |
dbSNP (classic) | rs28933402 |
ClinGen | rs28933402 |
ebi | rs28933402 |
HLI | rs28933402 |
Exac | rs28933402 |
Gnomad | rs28933402 |
Varsome | rs28933402 |
LitVar | rs28933402 |
Map | rs28933402 |
PheGenI | rs28933402 |
Biobank | rs28933402 |
1000 genomes | rs28933402 |
hgdp | rs28933402 |
ensembl | rs28933402 |
geneview | rs28933402 |
scholar | rs28933402 |
rs28933402 | |
pharmgkb | rs28933402 |
gwascentral | rs28933402 |
openSNP | rs28933402 |
23andMe | rs28933402 |
SNPshot | rs28933402 |
SNPdbe | rs28933402 |
MSV3d | rs28933402 |
GWAS Ctlg | rs28933402 |
Max Magnitude | 0 |
Leigh syndrome is more common in some French-Canadian populations. [PMID 12529507]
ClinVar | |
---|---|
Risk | rs28933402(A;A) |
Alt | rs28933402(A;A) |
Reference | Rs28933402(G;G) |
Significance | Pathogenic |
Disease | Congenital myasthenic syndrome |
Variation | info |
Gene | SURF1 |
CLNDBN | Congenital myasthenic syndrome, acetazolamide-responsive |
Reversed | 1 |
HGVS | NC_000009.11:g.136220748C>T |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000013606.17, |