rs543698823
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs543698823(-;A) |
Make rs543698823(A;A) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 4 |
Position | 16006637 |
Gene | PROM1 |
is a | snp |
is | mentioned by |
dbSNP | rs543698823 |
dbSNP (classic) | rs543698823 |
ClinGen | rs543698823 |
ebi | rs543698823 |
HLI | rs543698823 |
Exac | rs543698823 |
Gnomad | rs543698823 |
Varsome | rs543698823 |
LitVar | rs543698823 |
Map | rs543698823 |
PheGenI | rs543698823 |
Biobank | rs543698823 |
1000 genomes | rs543698823 |
hgdp | rs543698823 |
ensembl | rs543698823 |
geneview | rs543698823 |
scholar | rs543698823 |
rs543698823 | |
pharmgkb | rs543698823 |
gwascentral | rs543698823 |
openSNP | rs543698823 |
23andMe | rs543698823 |
SNPshot | rs543698823 |
SNPdbe | rs543698823 |
MSV3d | rs543698823 |
GWAS Ctlg | rs543698823 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs543698823(A;A) |
Alt | rs543698823(A;A) |
Reference | Rs543698823(-;-) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | PROM1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000004.11:g.16008261dupA |
CLNSRC | |
CLNACC | RCV000413568.1, |