rs773730492
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs773730492(C;T) |
Make rs773730492(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 15 |
Position | 84840372 |
Gene | ALPK3 |
is a | snp |
is | mentioned by |
dbSNP | rs773730492 |
dbSNP (classic) | rs773730492 |
ClinGen | rs773730492 |
ebi | rs773730492 |
HLI | rs773730492 |
Exac | rs773730492 |
Gnomad | rs773730492 |
Varsome | rs773730492 |
LitVar | rs773730492 |
Map | rs773730492 |
PheGenI | rs773730492 |
Biobank | rs773730492 |
1000 genomes | rs773730492 |
hgdp | rs773730492 |
ensembl | rs773730492 |
geneview | rs773730492 |
scholar | rs773730492 |
rs773730492 | |
pharmgkb | rs773730492 |
gwascentral | rs773730492 |
openSNP | rs773730492 |
23andMe | rs773730492 |
SNPshot | rs773730492 |
SNPdbe | rs773730492 |
MSV3d | rs773730492 |
GWAS Ctlg | rs773730492 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs773730492(T;T) |
Alt | rs773730492(T;T) |
Reference | Rs773730492(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | ALPK3 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000015.9:g.85383603C>T |
CLNSRC | |
CLNACC | RCV000478156.1, |