rs878854421
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs878854421(-;-) |
Make rs878854421(-;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 6 |
Position | 79025986 |
Gene | PHIP |
is a | snp |
is | mentioned by |
dbSNP | rs878854421 |
dbSNP (classic) | rs878854421 |
ClinGen | rs878854421 |
ebi | rs878854421 |
HLI | rs878854421 |
Exac | rs878854421 |
Gnomad | rs878854421 |
Varsome | rs878854421 |
LitVar | rs878854421 |
Map | rs878854421 |
PheGenI | rs878854421 |
Biobank | rs878854421 |
1000 genomes | rs878854421 |
hgdp | rs878854421 |
ensembl | rs878854421 |
geneview | rs878854421 |
scholar | rs878854421 |
rs878854421 | |
pharmgkb | rs878854421 |
gwascentral | rs878854421 |
openSNP | rs878854421 |
23andMe | rs878854421 |
SNPshot | rs878854421 |
SNPdbe | rs878854421 |
MSV3d | rs878854421 |
GWAS Ctlg | rs878854421 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs878854421(-;-) |
Alt | rs878854421(-;-) |
Reference | Rs878854421(T;T) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | PHIP |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000006.11:g.79735703delA |
CLNSRC | |
CLNACC | RCV000232097.1, |