rs28936072
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
(T;T) | 0 | common in clinvar |
Make rs28936072(C;C) |
Make rs28936072(C;T) |
Reference | GRCh38 38.1/142 |
Chromosome | X |
Position | 154765472 |
Gene | DKC1 |
is a | snp |
is | mentioned by |
dbSNP | rs28936072 |
dbSNP (classic) | rs28936072 |
ClinGen | rs28936072 |
ebi | rs28936072 |
HLI | rs28936072 |
Exac | rs28936072 |
Gnomad | rs28936072 |
Varsome | rs28936072 |
LitVar | rs28936072 |
Map | rs28936072 |
PheGenI | rs28936072 |
Biobank | rs28936072 |
1000 genomes | rs28936072 |
hgdp | rs28936072 |
ensembl | rs28936072 |
geneview | rs28936072 |
scholar | rs28936072 |
rs28936072 | |
pharmgkb | rs28936072 |
gwascentral | rs28936072 |
openSNP | rs28936072 |
23andMe | rs28936072 |
SNPshot | rs28936072 |
SNPdbe | rs28936072 |
MSV3d | rs28936072 |
GWAS Ctlg | rs28936072 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs28936072(G;G) |
Alt | rs28936072(G;G) |
Reference | Rs28936072(A;A) |
Significance | Pathogenic |
Disease | Hoyeraal Hreidarsson syndrome Dyskeratosis congenita X-linked |
Variation | info |
Gene | DKC1 |
CLNDBN | Hoyeraal Hreidarsson syndrome Dyskeratosis congenita X-linked |
Reversed | 1 |
HGVS | NC_000023.10:g.153993747T>C |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) UniProtKB (variants) |
CLNACC | RCV000012351.2, RCV000055631.25, |
[PMID 12437656] A novel DKC1 mutation, severe combined immunodeficiency (T+B-NK- SCID) and bone marrow transplantation in an infant with Hoyeraal-Hreidarsson syndrome.