rs587776625
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(CAGGACC;CAGGACC) | 0 | common in clinvar |
(CCAGGAC;CCAGGAC) | 0 | common in clinvar |
(I;I) | 0 | common genotype |
Make rs587776625(-;-) |
Make rs587776625(-;CAGGACC) |
Reference | GRCh38 38.1/142 |
Chromosome | 16 |
Position | 57654104 |
Gene | ADGRG1 |
is a | snp |
is | mentioned by |
dbSNP | rs587776625 |
dbSNP (classic) | rs587776625 |
ClinGen | rs587776625 |
ebi | rs587776625 |
HLI | rs587776625 |
Exac | rs587776625 |
Gnomad | rs587776625 |
Varsome | rs587776625 |
LitVar | rs587776625 |
Map | rs587776625 |
PheGenI | rs587776625 |
Biobank | rs587776625 |
1000 genomes | rs587776625 |
hgdp | rs587776625 |
ensembl | rs587776625 |
geneview | rs587776625 |
scholar | rs587776625 |
rs587776625 | |
pharmgkb | rs587776625 |
gwascentral | rs587776625 |
openSNP | rs587776625 |
23andMe | rs587776625 |
SNPshot | rs587776625 |
SNPdbe | rs587776625 |
MSV3d | rs587776625 |
GWAS Ctlg | rs587776625 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587776625(-;-) Rs587776625(CCAGGAC;CCAGGAC) |
Alt | rs587776625(-;-) Rs587776625(CCAGGAC;CCAGGAC) |
Reference | Rs587776625(CAGGACC;CAGGACC) |
Significance | Pathogenic |
Disease | Polymicrogyria not provided |
Variation | info |
Gene | ADGRG1 GPR56 |
CLNDBN | Polymicrogyria, bilateral frontoparietal not provided |
Reversed | 0 |
HGVS | NC_000016.9:g.57688016_57688022delCAGGACC |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000006184.5, RCV000351326.1, |