rs796052689
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs796052689(C;C) |
Make rs796052689(C;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 7 |
Position | 66639066 |
Gene | KCTD7 |
is a | snp |
is | mentioned by |
dbSNP | rs796052689 |
dbSNP (classic) | rs796052689 |
ClinGen | rs796052689 |
ebi | rs796052689 |
HLI | rs796052689 |
Exac | rs796052689 |
Gnomad | rs796052689 |
Varsome | rs796052689 |
LitVar | rs796052689 |
Map | rs796052689 |
PheGenI | rs796052689 |
Biobank | rs796052689 |
1000 genomes | rs796052689 |
hgdp | rs796052689 |
ensembl | rs796052689 |
geneview | rs796052689 |
scholar | rs796052689 |
rs796052689 | |
pharmgkb | rs796052689 |
gwascentral | rs796052689 |
openSNP | rs796052689 |
23andMe | rs796052689 |
SNPshot | rs796052689 |
SNPdbe | rs796052689 |
MSV3d | rs796052689 |
GWAS Ctlg | rs796052689 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs796052689(C;C) |
Alt | rs796052689(C;C) |
Reference | Rs796052689(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | KCTD7 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000007.13:g.66104053G>C |
CLNSRC | |
CLNACC | RCV000188025.2, |