rs370072439
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs370072439(G;T) |
Make rs370072439(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 15 |
Position | 84840114 |
Gene | ALPK3 |
is a | snp |
is | mentioned by |
dbSNP | rs370072439 |
dbSNP (classic) | rs370072439 |
ClinGen | rs370072439 |
ebi | rs370072439 |
HLI | rs370072439 |
Exac | rs370072439 |
Gnomad | rs370072439 |
Varsome | rs370072439 |
LitVar | rs370072439 |
Map | rs370072439 |
PheGenI | rs370072439 |
Biobank | rs370072439 |
1000 genomes | rs370072439 |
hgdp | rs370072439 |
ensembl | rs370072439 |
geneview | rs370072439 |
scholar | rs370072439 |
rs370072439 | |
pharmgkb | rs370072439 |
gwascentral | rs370072439 |
openSNP | rs370072439 |
23andMe | rs370072439 |
SNPshot | rs370072439 |
SNPdbe | rs370072439 |
MSV3d | rs370072439 |
GWAS Ctlg | rs370072439 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs370072439(T;T) |
Alt | rs370072439(T;T) |
Reference | Rs370072439(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | ALPK3 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000015.9:g.85383345G>T |
CLNSRC | |
CLNACC | RCV000428802.1, |