rs148932047
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs148932047(A;A) |
Make rs148932047(A;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 10 |
Position | 77993367 |
Gene | POLR3A |
is a | snp |
is | mentioned by |
dbSNP | rs148932047 |
dbSNP (classic) | rs148932047 |
ClinGen | rs148932047 |
ebi | rs148932047 |
HLI | rs148932047 |
Exac | rs148932047 |
Gnomad | rs148932047 |
Varsome | rs148932047 |
LitVar | rs148932047 |
Map | rs148932047 |
PheGenI | rs148932047 |
Biobank | rs148932047 |
1000 genomes | rs148932047 |
hgdp | rs148932047 |
ensembl | rs148932047 |
geneview | rs148932047 |
scholar | rs148932047 |
rs148932047 | |
pharmgkb | rs148932047 |
gwascentral | rs148932047 |
openSNP | rs148932047 |
23andMe | rs148932047 |
SNPshot | rs148932047 |
SNPdbe | rs148932047 |
MSV3d | rs148932047 |
GWAS Ctlg | rs148932047 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs148932047(A;A) |
Alt | rs148932047(A;A) |
Reference | Rs148932047(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | POLR3A |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000010.10:g.79753125G>A |
CLNSRC | |
CLNACC | RCV000224488.1, |