rs747912710
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs747912710(A;G) |
Make rs747912710(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 12 |
Position | 106454496 |
Gene | POLR3B |
is a | snp |
is | mentioned by |
dbSNP | rs747912710 |
dbSNP (classic) | rs747912710 |
ClinGen | rs747912710 |
ebi | rs747912710 |
HLI | rs747912710 |
Exac | rs747912710 |
Gnomad | rs747912710 |
Varsome | rs747912710 |
LitVar | rs747912710 |
Map | rs747912710 |
PheGenI | rs747912710 |
Biobank | rs747912710 |
1000 genomes | rs747912710 |
hgdp | rs747912710 |
ensembl | rs747912710 |
geneview | rs747912710 |
scholar | rs747912710 |
rs747912710 | |
pharmgkb | rs747912710 |
gwascentral | rs747912710 |
openSNP | rs747912710 |
23andMe | rs747912710 |
SNPshot | rs747912710 |
SNPdbe | rs747912710 |
MSV3d | rs747912710 |
GWAS Ctlg | rs747912710 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs747912710(G;G) |
Alt | rs747912710(G;G) |
Reference | Rs747912710(A;A) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | POLR3B |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000012.11:g.106848274A>G |
CLNSRC | |
CLNACC | RCV000484819.1, |