rs199476393
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common genotype |
(GC;GC) | 0 | common in clinvar |
Make rs199476393(AG;AG) |
Make rs199476393(AG;GC) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 169764953 |
Gene | TERC |
is a | snp |
is | mentioned by |
dbSNP | rs199476393 |
dbSNP (classic) | rs199476393 |
ClinGen | rs199476393 |
ebi | rs199476393 |
HLI | rs199476393 |
Exac | rs199476393 |
Gnomad | rs199476393 |
Varsome | rs199476393 |
LitVar | rs199476393 |
Map | rs199476393 |
PheGenI | rs199476393 |
Biobank | rs199476393 |
1000 genomes | rs199476393 |
hgdp | rs199476393 |
ensembl | rs199476393 |
geneview | rs199476393 |
scholar | rs199476393 |
rs199476393 | |
pharmgkb | rs199476393 |
gwascentral | rs199476393 |
openSNP | rs199476393 |
23andMe | rs199476393 |
SNPshot | rs199476393 |
SNPdbe | rs199476393 |
MSV3d | rs199476393 |
GWAS Ctlg | rs199476393 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs199476393(AG;AG) |
Alt | rs199476393(AG;AG) |
Reference | Rs199476393(GC;GC) |
Significance | Pathogenic |
Disease | Dyskeratosis congenita autosomal dominant |
Variation | info |
Gene | TERC |
CLNDBN | Dyskeratosis congenita autosomal dominant |
Reversed | 1 |
HGVS | NC_000003.11:g.169482741_169482742delGCinsCT |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000007745.4, |