rs772727116
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs772727116(C;T) |
Make rs772727116(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 19 |
Position | 49862408 |
Gene | PNKP |
is a | snp |
is | mentioned by |
dbSNP | rs772727116 |
dbSNP (classic) | rs772727116 |
ClinGen | rs772727116 |
ebi | rs772727116 |
HLI | rs772727116 |
Exac | rs772727116 |
Gnomad | rs772727116 |
Varsome | rs772727116 |
LitVar | rs772727116 |
Map | rs772727116 |
PheGenI | rs772727116 |
Biobank | rs772727116 |
1000 genomes | rs772727116 |
hgdp | rs772727116 |
ensembl | rs772727116 |
geneview | rs772727116 |
scholar | rs772727116 |
rs772727116 | |
pharmgkb | rs772727116 |
gwascentral | rs772727116 |
openSNP | rs772727116 |
23andMe | rs772727116 |
SNPshot | rs772727116 |
SNPdbe | rs772727116 |
MSV3d | rs772727116 |
GWAS Ctlg | rs772727116 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs772727116(T;T) |
Alt | rs772727116(T;T) |
Reference | Rs772727116(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | PNKP |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000019.9:g.50365665C>T |
CLNSRC | |
CLNACC | RCV000188442.2, |