rs767074039
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs767074039(G;G) |
Make rs767074039(G;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 10 |
Position | 8064004 |
Gene | GATA3 |
is a | snp |
is | mentioned by |
dbSNP | rs767074039 |
dbSNP (classic) | rs767074039 |
ClinGen | rs767074039 |
ebi | rs767074039 |
HLI | rs767074039 |
Exac | rs767074039 |
Gnomad | rs767074039 |
Varsome | rs767074039 |
LitVar | rs767074039 |
Map | rs767074039 |
PheGenI | rs767074039 |
Biobank | rs767074039 |
1000 genomes | rs767074039 |
hgdp | rs767074039 |
ensembl | rs767074039 |
geneview | rs767074039 |
scholar | rs767074039 |
rs767074039 | |
pharmgkb | rs767074039 |
gwascentral | rs767074039 |
openSNP | rs767074039 |
23andMe | rs767074039 |
SNPshot | rs767074039 |
SNPdbe | rs767074039 |
MSV3d | rs767074039 |
GWAS Ctlg | rs767074039 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs767074039(C;C) rs767074039(G;G) |
Alt | rs767074039(C;C) rs767074039(G;G) |
Reference | Rs767074039(T;T) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | GATA3 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000010.10:g.8105967T>C |
CLNSRC | |
CLNACC | RCV000485463.1, |