rs797045264
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs797045264(C;C) |
Make rs797045264(C;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 1 |
Position | 26779036 |
Gene | ARID1A |
is a | snp |
is | mentioned by |
dbSNP | rs797045264 |
dbSNP (classic) | rs797045264 |
ClinGen | rs797045264 |
ebi | rs797045264 |
HLI | rs797045264 |
Exac | rs797045264 |
Gnomad | rs797045264 |
Varsome | rs797045264 |
LitVar | rs797045264 |
Map | rs797045264 |
PheGenI | rs797045264 |
Biobank | rs797045264 |
1000 genomes | rs797045264 |
hgdp | rs797045264 |
ensembl | rs797045264 |
geneview | rs797045264 |
scholar | rs797045264 |
rs797045264 | |
pharmgkb | rs797045264 |
gwascentral | rs797045264 |
openSNP | rs797045264 |
23andMe | rs797045264 |
SNPshot | rs797045264 |
SNPdbe | rs797045264 |
MSV3d | rs797045264 |
GWAS Ctlg | rs797045264 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs797045264(C;C) |
Alt | rs797045264(C;C) |
Reference | Rs797045264(T;T) |
Significance | Probable-Pathogenic |
Disease | Mental retardation |
Variation | info |
Gene | ARID1A |
CLNDBN | Mental retardation, autosomal dominant 14 |
Reversed | 0 |
HGVS | NC_000001.10:g.27105527T>C |
CLNSRC | |
CLNACC | RCV000194434.1, |