rs864321628
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 8.3 | Mental retardation, syndromic 33, X-linked |
(C;T) | 3 | Carrier of a mutation for an X-linked form of mental retardation, syndromic 33 |
(T;T) | 0 | common in clinvar |
Reference | GRCh38.p2 38.2/147 |
Chromosome | X |
Position | 71387393 |
Gene | TAF1 |
is a | snp |
is | mentioned by |
dbSNP | rs864321628 |
dbSNP (classic) | rs864321628 |
ClinGen | rs864321628 |
ebi | rs864321628 |
HLI | rs864321628 |
Exac | rs864321628 |
Gnomad | rs864321628 |
Varsome | rs864321628 |
LitVar | rs864321628 |
Map | rs864321628 |
PheGenI | rs864321628 |
Biobank | rs864321628 |
1000 genomes | rs864321628 |
hgdp | rs864321628 |
ensembl | rs864321628 |
geneview | rs864321628 |
scholar | rs864321628 |
rs864321628 | |
pharmgkb | rs864321628 |
gwascentral | rs864321628 |
openSNP | rs864321628 |
23andMe | rs864321628 |
SNPshot | rs864321628 |
SNPdbe | rs864321628 |
MSV3d | rs864321628 |
GWAS Ctlg | rs864321628 |
Max Magnitude | 8.3 |
c.2419T>C (p.Cys807Arg)
ClinVar | |
---|---|
Risk | Rs864321628(C;C) |
Alt | Rs864321628(C;C) |
Reference | Rs864321628(T;T) |
Significance | Pathogenic |
Disease | Mental retardation |
Variation | info |
Gene | TAF1 |
CLNDBN | Mental retardation, X-linked, syndromic 33 |
Reversed | 0 |
HGVS | NC_000023.10:g.70607243T>C |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000203551.2, |