rs878853147
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs878853147(C;T) |
Make rs878853147(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | X |
Position | 71169399 |
Gene | NLGN3 |
is a | snp |
is | mentioned by |
dbSNP | rs878853147 |
dbSNP (classic) | rs878853147 |
ClinGen | rs878853147 |
ebi | rs878853147 |
HLI | rs878853147 |
Exac | rs878853147 |
Gnomad | rs878853147 |
Varsome | rs878853147 |
LitVar | rs878853147 |
Map | rs878853147 |
PheGenI | rs878853147 |
Biobank | rs878853147 |
1000 genomes | rs878853147 |
hgdp | rs878853147 |
ensembl | rs878853147 |
geneview | rs878853147 |
scholar | rs878853147 |
rs878853147 | |
pharmgkb | rs878853147 |
gwascentral | rs878853147 |
openSNP | rs878853147 |
23andMe | rs878853147 |
SNPshot | rs878853147 |
SNPdbe | rs878853147 |
MSV3d | rs878853147 |
GWAS Ctlg | rs878853147 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs878853147(T;T) |
Alt | rs878853147(T;T) |
Reference | Rs878853147(C;C) |
Significance | Probable-Pathogenic |
Disease | Intellectual disability |
Variation | info |
Gene | NLGN3 |
CLNDBN | Intellectual disability |
Reversed | 0 |
HGVS | NC_000023.10:g.70389249C>T |
CLNSRC | |
CLNACC | RCV000224769.1, |