rs104894163
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs104894163(A;A) |
Make rs104894163(A;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 10 |
Position | 8064037 |
Gene | GATA3 |
is a | snp |
is | mentioned by |
dbSNP | rs104894163 |
dbSNP (classic) | rs104894163 |
ClinGen | rs104894163 |
ebi | rs104894163 |
HLI | rs104894163 |
Exac | rs104894163 |
Gnomad | rs104894163 |
Varsome | rs104894163 |
LitVar | rs104894163 |
Map | rs104894163 |
PheGenI | rs104894163 |
Biobank | rs104894163 |
1000 genomes | rs104894163 |
hgdp | rs104894163 |
ensembl | rs104894163 |
geneview | rs104894163 |
scholar | rs104894163 |
rs104894163 | |
pharmgkb | rs104894163 |
gwascentral | rs104894163 |
openSNP | rs104894163 |
23andMe | rs104894163 |
SNPshot | rs104894163 |
SNPdbe | rs104894163 |
MSV3d | rs104894163 |
GWAS Ctlg | rs104894163 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs104894163(A;A) |
Alt | rs104894163(A;A) |
Reference | Rs104894163(T;T) |
Significance | Pathogenic |
Disease | Barakat syndrome |
Variation | info |
Gene | GATA3 |
CLNDBN | Barakat syndrome |
Reversed | 0 |
HGVS | NC_000010.10:g.8106000T>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000018103.28, |