rs772731615
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs772731615(C;T) |
Make rs772731615(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 14 |
Position | 96860628 |
Gene | VRK1 |
is a | snp |
is | mentioned by |
dbSNP | rs772731615 |
dbSNP (classic) | rs772731615 |
ClinGen | rs772731615 |
ebi | rs772731615 |
HLI | rs772731615 |
Exac | rs772731615 |
Gnomad | rs772731615 |
Varsome | rs772731615 |
LitVar | rs772731615 |
Map | rs772731615 |
PheGenI | rs772731615 |
Biobank | rs772731615 |
1000 genomes | rs772731615 |
hgdp | rs772731615 |
ensembl | rs772731615 |
geneview | rs772731615 |
scholar | rs772731615 |
rs772731615 | |
pharmgkb | rs772731615 |
gwascentral | rs772731615 |
openSNP | rs772731615 |
23andMe | rs772731615 |
SNPshot | rs772731615 |
SNPdbe | rs772731615 |
MSV3d | rs772731615 |
GWAS Ctlg | rs772731615 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs772731615(T;T) |
Alt | rs772731615(T;T) |
Reference | Rs772731615(C;C) |
Significance | Probable-Pathogenic |
Disease | Pontocerebellar hypoplasia type 1A not specified |
Variation | info |
Gene | VRK1 |
CLNDBN | Pontocerebellar hypoplasia type 1A not specified |
Reversed | 0 |
HGVS | NC_000014.8:g.97326965C>T |
CLNSRC | Baylor College of Medicine |
CLNACC | RCV000191144.1, RCV000435348.1, |