rs755165065
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs755165065(C;T) |
Make rs755165065(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 10 |
Position | 78007846 |
Gene | POLR3A |
is a | snp |
is | mentioned by |
dbSNP | rs755165065 |
dbSNP (classic) | rs755165065 |
ClinGen | rs755165065 |
ebi | rs755165065 |
HLI | rs755165065 |
Exac | rs755165065 |
Gnomad | rs755165065 |
Varsome | rs755165065 |
LitVar | rs755165065 |
Map | rs755165065 |
PheGenI | rs755165065 |
Biobank | rs755165065 |
1000 genomes | rs755165065 |
hgdp | rs755165065 |
ensembl | rs755165065 |
geneview | rs755165065 |
scholar | rs755165065 |
rs755165065 | |
pharmgkb | rs755165065 |
gwascentral | rs755165065 |
openSNP | rs755165065 |
23andMe | rs755165065 |
SNPshot | rs755165065 |
SNPdbe | rs755165065 |
MSV3d | rs755165065 |
GWAS Ctlg | rs755165065 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs755165065(T;T) |
Alt | rs755165065(T;T) |
Reference | Rs755165065(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | POLR3A |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000010.10:g.79767604C>T |
CLNSRC | |
CLNACC | RCV000414392.1, |