rs886039742
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs886039742(-;-) |
Make rs886039742(-;G) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 10 |
Position | 74843114 |
Gene | KAT6B |
is a | snp |
is | mentioned by |
dbSNP | rs886039742 |
dbSNP (classic) | rs886039742 |
ClinGen | rs886039742 |
ebi | rs886039742 |
HLI | rs886039742 |
Exac | rs886039742 |
Gnomad | rs886039742 |
Varsome | rs886039742 |
LitVar | rs886039742 |
Map | rs886039742 |
PheGenI | rs886039742 |
Biobank | rs886039742 |
1000 genomes | rs886039742 |
hgdp | rs886039742 |
ensembl | rs886039742 |
geneview | rs886039742 |
scholar | rs886039742 |
rs886039742 | |
pharmgkb | rs886039742 |
gwascentral | rs886039742 |
openSNP | rs886039742 |
23andMe | rs886039742 |
SNPshot | rs886039742 |
SNPdbe | rs886039742 |
MSV3d | rs886039742 |
GWAS Ctlg | rs886039742 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs886039742(-;-) |
Alt | rs886039742(-;-) |
Reference | Rs886039742(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | KAT6B |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000010.10:g.76602872delG |
CLNSRC | |
CLNACC | RCV000255091.1, |