rs797045262
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(CCCGCCGCCGCCAGCAGCCTGGGCAA;CCCGCCGCCGCCAGCAGCCTGGGCAA) | 0 | common in clinvar |
Make rs797045262(-;-) |
Make rs797045262(-;AGCAGCCTGGGCAACCCGCCGCCGCC) |
Make rs797045262(AGCAGCCTGGGCAACCCGCCGCCGCC;AGCAGCCTGGGCAACCCGCCGCCGCC) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 1 |
Position | 26696434 |
Gene | ARID1A |
is a | snp |
is | mentioned by |
dbSNP | rs797045262 |
dbSNP (classic) | rs797045262 |
ClinGen | rs797045262 |
ebi | rs797045262 |
HLI | rs797045262 |
Exac | rs797045262 |
Gnomad | rs797045262 |
Varsome | rs797045262 |
LitVar | rs797045262 |
Map | rs797045262 |
PheGenI | rs797045262 |
Biobank | rs797045262 |
1000 genomes | rs797045262 |
hgdp | rs797045262 |
ensembl | rs797045262 |
geneview | rs797045262 |
scholar | rs797045262 |
rs797045262 | |
pharmgkb | rs797045262 |
gwascentral | rs797045262 |
openSNP | rs797045262 |
23andMe | rs797045262 |
SNPshot | rs797045262 |
SNPdbe | rs797045262 |
MSV3d | rs797045262 |
GWAS Ctlg | rs797045262 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs797045262(-;-) |
Alt | rs797045262(-;-) |
Reference | Rs797045262(CCCGCCGCCGCCAGCAGCCTGGGCAA;CCCGCCGCCGCCAGCAGCCTGGGCAA) |
Significance | Pathogenic |
Disease | Mental retardation not provided |
Variation | info |
Gene | LOC101928728 ARID1A |
CLNDBN | Mental retardation, autosomal dominant 14 not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.27022925_27022950del26 |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000023227.4, RCV000480869.1, |