rs765815715
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs765815715(C;C) |
Make rs765815715(C;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 20 |
Position | 61928394 |
Gene | CDH4 |
is a | snp |
is | mentioned by |
dbSNP | rs765815715 |
dbSNP (classic) | rs765815715 |
ClinGen | rs765815715 |
ebi | rs765815715 |
HLI | rs765815715 |
Exac | rs765815715 |
Gnomad | rs765815715 |
Varsome | rs765815715 |
LitVar | rs765815715 |
Map | rs765815715 |
PheGenI | rs765815715 |
Biobank | rs765815715 |
1000 genomes | rs765815715 |
hgdp | rs765815715 |
ensembl | rs765815715 |
geneview | rs765815715 |
scholar | rs765815715 |
rs765815715 | |
pharmgkb | rs765815715 |
gwascentral | rs765815715 |
openSNP | rs765815715 |
23andMe | rs765815715 |
SNPshot | rs765815715 |
SNPdbe | rs765815715 |
MSV3d | rs765815715 |
GWAS Ctlg | rs765815715 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs765815715(A;A) rs765815715(C;C) |
Alt | rs765815715(A;A) rs765815715(C;C) |
Reference | Rs765815715(G;G) |
Significance | Probable-Pathogenic |
Disease | Abnormality of brain morphology |
Variation | info |
Gene | CDH4 |
CLNDBN | Abnormality of brain morphology |
Reversed | 0 |
HGVS | NC_000020.10:g.60503452G>C |
CLNSRC | |
CLNACC | RCV000454293.1, |