rs770674400
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs770674400(G;T) |
Make rs770674400(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 10 |
Position | 75022145 |
Gene | KAT6B, SNORD172 |
is a | snp |
is | mentioned by |
dbSNP | rs770674400 |
dbSNP (classic) | rs770674400 |
ClinGen | rs770674400 |
ebi | rs770674400 |
HLI | rs770674400 |
Exac | rs770674400 |
Gnomad | rs770674400 |
Varsome | rs770674400 |
LitVar | rs770674400 |
Map | rs770674400 |
PheGenI | rs770674400 |
Biobank | rs770674400 |
1000 genomes | rs770674400 |
hgdp | rs770674400 |
ensembl | rs770674400 |
geneview | rs770674400 |
scholar | rs770674400 |
rs770674400 | |
pharmgkb | rs770674400 |
gwascentral | rs770674400 |
openSNP | rs770674400 |
23andMe | rs770674400 |
SNPshot | rs770674400 |
SNPdbe | rs770674400 |
MSV3d | rs770674400 |
GWAS Ctlg | rs770674400 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs770674400(A;A) rs770674400(T;T) |
Alt | rs770674400(A;A) rs770674400(T;T) |
Reference | Rs770674400(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | KAT6B |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000010.10:g.76781903G>T |
CLNSRC | |
CLNACC | RCV000484958.1, |