rs587776908
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs587776908(C;T) |
Make rs587776908(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 5 |
Position | 6600195 |
Gene | NSUN2 |
is a | snp |
is | mentioned by |
dbSNP | rs587776908 |
dbSNP (classic) | rs587776908 |
ClinGen | rs587776908 |
ebi | rs587776908 |
HLI | rs587776908 |
Exac | rs587776908 |
Gnomad | rs587776908 |
Varsome | rs587776908 |
LitVar | rs587776908 |
Map | rs587776908 |
PheGenI | rs587776908 |
Biobank | rs587776908 |
1000 genomes | rs587776908 |
hgdp | rs587776908 |
ensembl | rs587776908 |
geneview | rs587776908 |
scholar | rs587776908 |
rs587776908 | |
pharmgkb | rs587776908 |
gwascentral | rs587776908 |
openSNP | rs587776908 |
23andMe | rs587776908 |
SNPshot | rs587776908 |
SNPdbe | rs587776908 |
MSV3d | rs587776908 |
GWAS Ctlg | rs587776908 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587776908(T;T) |
Alt | rs587776908(T;T) |
Reference | Rs587776908(C;C) |
Significance | Pathogenic |
Disease | Mental retardation |
Variation | info |
Gene | NSUN2 |
CLNDBN | Mental retardation, autosomal recessive 5 |
Reversed | 0 |
HGVS | NC_000005.9:g.6600308C>T |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000024358.2, |