rs879255541
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs879255541(-;G) |
Make rs879255541(G;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 19 |
Position | 49865359 |
Gene | PNKP |
is a | snp |
is | mentioned by |
dbSNP | rs879255541 |
dbSNP (classic) | rs879255541 |
ClinGen | rs879255541 |
ebi | rs879255541 |
HLI | rs879255541 |
Exac | rs879255541 |
Gnomad | rs879255541 |
Varsome | rs879255541 |
LitVar | rs879255541 |
Map | rs879255541 |
PheGenI | rs879255541 |
Biobank | rs879255541 |
1000 genomes | rs879255541 |
hgdp | rs879255541 |
ensembl | rs879255541 |
geneview | rs879255541 |
scholar | rs879255541 |
rs879255541 | |
pharmgkb | rs879255541 |
gwascentral | rs879255541 |
openSNP | rs879255541 |
23andMe | rs879255541 |
SNPshot | rs879255541 |
SNPdbe | rs879255541 |
MSV3d | rs879255541 |
GWAS Ctlg | rs879255541 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs879255541(G;G) |
Alt | rs879255541(G;G) |
Reference | Rs879255541(-;-) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | PNKP |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000019.9:g.50368617dupC |
CLNSRC | |
CLNACC | RCV000224524.1, |