rs796052388
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs796052388(-;-) |
Make rs796052388(-;A) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 7 |
Position | 147121075 |
Gene | CNTNAP2 |
is a | snp |
is | mentioned by |
dbSNP | rs796052388 |
dbSNP (classic) | rs796052388 |
ClinGen | rs796052388 |
ebi | rs796052388 |
HLI | rs796052388 |
Exac | rs796052388 |
Gnomad | rs796052388 |
Varsome | rs796052388 |
LitVar | rs796052388 |
Map | rs796052388 |
PheGenI | rs796052388 |
Biobank | rs796052388 |
1000 genomes | rs796052388 |
hgdp | rs796052388 |
ensembl | rs796052388 |
geneview | rs796052388 |
scholar | rs796052388 |
rs796052388 | |
pharmgkb | rs796052388 |
gwascentral | rs796052388 |
openSNP | rs796052388 |
23andMe | rs796052388 |
SNPshot | rs796052388 |
SNPdbe | rs796052388 |
MSV3d | rs796052388 |
GWAS Ctlg | rs796052388 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs796052388(-;-) |
Alt | rs796052388(-;-) |
Reference | Rs796052388(A;A) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | CNTNAP2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000007.13:g.146818167delA |
CLNSRC | |
CLNACC | RCV000187252.1, |