rs796052345
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(CT;CT) | 0 | common in clinvar |
Make rs796052345(-;-) |
Make rs796052345(-;CT) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 13 |
Position | 77000959 |
Gene | CLN5, FBXL3 |
is a | snp |
is | mentioned by |
dbSNP | rs796052345 |
dbSNP (classic) | rs796052345 |
ClinGen | rs796052345 |
ebi | rs796052345 |
HLI | rs796052345 |
Exac | rs796052345 |
Gnomad | rs796052345 |
Varsome | rs796052345 |
LitVar | rs796052345 |
Map | rs796052345 |
PheGenI | rs796052345 |
Biobank | rs796052345 |
1000 genomes | rs796052345 |
hgdp | rs796052345 |
ensembl | rs796052345 |
geneview | rs796052345 |
scholar | rs796052345 |
rs796052345 | |
pharmgkb | rs796052345 |
gwascentral | rs796052345 |
openSNP | rs796052345 |
23andMe | rs796052345 |
SNPshot | rs796052345 |
SNPdbe | rs796052345 |
MSV3d | rs796052345 |
GWAS Ctlg | rs796052345 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs796052345(-;-) |
Alt | rs796052345(-;-) |
Reference | Rs796052345(CT;CT) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | CLN5 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000013.10:g.77575094_77575095delCT |
CLNSRC | |
CLNACC | RCV000187074.1, |