rs199504211
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs199504211(C;C) |
Make rs199504211(C;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 12 |
Position | 106427339 |
Gene | POLR3B |
is a | snp |
is | mentioned by |
dbSNP | rs199504211 |
dbSNP (classic) | rs199504211 |
ClinGen | rs199504211 |
ebi | rs199504211 |
HLI | rs199504211 |
Exac | rs199504211 |
Gnomad | rs199504211 |
Varsome | rs199504211 |
LitVar | rs199504211 |
Map | rs199504211 |
PheGenI | rs199504211 |
Biobank | rs199504211 |
1000 genomes | rs199504211 |
hgdp | rs199504211 |
ensembl | rs199504211 |
geneview | rs199504211 |
scholar | rs199504211 |
rs199504211 | |
pharmgkb | rs199504211 |
gwascentral | rs199504211 |
openSNP | rs199504211 |
23andMe | rs199504211 |
SNPshot | rs199504211 |
SNPdbe | rs199504211 |
MSV3d | rs199504211 |
GWAS Ctlg | rs199504211 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs199504211(C;C) |
Alt | rs199504211(C;C) |
Reference | Rs199504211(T;T) |
Significance | Pathogenic |
Disease | not specified not provided |
Variation | info |
Gene | POLR3B |
CLNDBN | not specified not provided |
Reversed | 0 |
HGVS | NC_000012.11:g.106821117T>C |
CLNSRC | |
CLNACC | RCV000372557.1, RCV000427637.1, |