rs771317809
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs771317809(C;T) |
Make rs771317809(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 7 |
Position | 50470140 |
Gene | DDC |
is a | snp |
is | mentioned by |
dbSNP | rs771317809 |
dbSNP (classic) | rs771317809 |
ClinGen | rs771317809 |
ebi | rs771317809 |
HLI | rs771317809 |
Exac | rs771317809 |
Gnomad | rs771317809 |
Varsome | rs771317809 |
LitVar | rs771317809 |
Map | rs771317809 |
PheGenI | rs771317809 |
Biobank | rs771317809 |
1000 genomes | rs771317809 |
hgdp | rs771317809 |
ensembl | rs771317809 |
geneview | rs771317809 |
scholar | rs771317809 |
rs771317809 | |
pharmgkb | rs771317809 |
gwascentral | rs771317809 |
openSNP | rs771317809 |
23andMe | rs771317809 |
SNPshot | rs771317809 |
SNPdbe | rs771317809 |
MSV3d | rs771317809 |
GWAS Ctlg | rs771317809 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs771317809(T;T) |
Alt | rs771317809(T;T) |
Reference | Rs771317809(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | DDC |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000007.13:g.50537838C>T |
CLNSRC | |
CLNACC | RCV000445005.1, |