rs879255535
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs879255535(-;-) |
Make rs879255535(-;C) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 10 |
Position | 60069886 |
Gene | ANK3 |
is a | snp |
is | mentioned by |
dbSNP | rs879255535 |
dbSNP (classic) | rs879255535 |
ClinGen | rs879255535 |
ebi | rs879255535 |
HLI | rs879255535 |
Exac | rs879255535 |
Gnomad | rs879255535 |
Varsome | rs879255535 |
LitVar | rs879255535 |
Map | rs879255535 |
PheGenI | rs879255535 |
Biobank | rs879255535 |
1000 genomes | rs879255535 |
hgdp | rs879255535 |
ensembl | rs879255535 |
geneview | rs879255535 |
scholar | rs879255535 |
rs879255535 | |
pharmgkb | rs879255535 |
gwascentral | rs879255535 |
openSNP | rs879255535 |
23andMe | rs879255535 |
SNPshot | rs879255535 |
SNPdbe | rs879255535 |
MSV3d | rs879255535 |
GWAS Ctlg | rs879255535 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs879255535(-;-) |
Alt | rs879255535(-;-) |
Reference | Rs879255535(C;C) |
Significance | Pathogenic |
Disease | Mental retardation |
Variation | info |
Gene | ANK3 |
CLNDBN | Mental retardation, autosomal recessive 37 |
Reversed | 1 |
HGVS | NC_000010.10:g.61829644delG |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000074342.2, |