rs869312678
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(TG;TG) | 0 | common in clinvar |
Make rs869312678(-;-) |
Make rs869312678(-;TG) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 22 |
Position | 42209920 |
Gene | TCF20 |
is a | snp |
is | mentioned by |
dbSNP | rs869312678 |
dbSNP (classic) | rs869312678 |
ClinGen | rs869312678 |
ebi | rs869312678 |
HLI | rs869312678 |
Exac | rs869312678 |
Gnomad | rs869312678 |
Varsome | rs869312678 |
LitVar | rs869312678 |
Map | rs869312678 |
PheGenI | rs869312678 |
Biobank | rs869312678 |
1000 genomes | rs869312678 |
hgdp | rs869312678 |
ensembl | rs869312678 |
geneview | rs869312678 |
scholar | rs869312678 |
rs869312678 | |
pharmgkb | rs869312678 |
gwascentral | rs869312678 |
openSNP | rs869312678 |
23andMe | rs869312678 |
SNPshot | rs869312678 |
SNPdbe | rs869312678 |
MSV3d | rs869312678 |
GWAS Ctlg | rs869312678 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs869312678(-;-) |
Alt | rs869312678(-;-) |
Reference | Rs869312678(TG;TG) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | TCF20 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000022.10:g.42605926_42605927delCA |
CLNSRC | |
CLNACC | RCV000209874.3, |