rs797044894
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs797044894(-;G) |
Make rs797044894(G;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 10 |
Position | 75028925 |
Gene | DUPD1, KAT6B |
is a | snp |
is | mentioned by |
dbSNP | rs797044894 |
dbSNP (classic) | rs797044894 |
ClinGen | rs797044894 |
ebi | rs797044894 |
HLI | rs797044894 |
Exac | rs797044894 |
Gnomad | rs797044894 |
Varsome | rs797044894 |
LitVar | rs797044894 |
Map | rs797044894 |
PheGenI | rs797044894 |
Biobank | rs797044894 |
1000 genomes | rs797044894 |
hgdp | rs797044894 |
ensembl | rs797044894 |
geneview | rs797044894 |
scholar | rs797044894 |
rs797044894 | |
pharmgkb | rs797044894 |
gwascentral | rs797044894 |
openSNP | rs797044894 |
23andMe | rs797044894 |
SNPshot | rs797044894 |
SNPdbe | rs797044894 |
MSV3d | rs797044894 |
GWAS Ctlg | rs797044894 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs797044894(G;G) |
Alt | rs797044894(G;G) |
Reference | Rs797044894(-;-) |
Significance | Pathogenic |
Disease | Inborn genetic diseases |
Variation | info |
Gene | KAT6B |
CLNDBN | Inborn genetic diseases |
Reversed | 0 |
HGVS | NC_000010.10:g.76788683dupG |
CLNSRC | |
CLNACC | RCV000190717.1, |