rs387906631
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common genotype |
Make rs387906631(C;T) |
Make rs387906631(T;T) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 3 |
Position | 128481901 |
Gene | GATA2 |
is a | snp |
is | mentioned by |
dbSNP | rs387906631 |
dbSNP (classic) | rs387906631 |
ClinGen | rs387906631 |
ebi | rs387906631 |
HLI | rs387906631 |
Exac | rs387906631 |
Gnomad | rs387906631 |
Varsome | rs387906631 |
LitVar | rs387906631 |
Map | rs387906631 |
PheGenI | rs387906631 |
Biobank | rs387906631 |
1000 genomes | rs387906631 |
hgdp | rs387906631 |
ensembl | rs387906631 |
geneview | rs387906631 |
scholar | rs387906631 |
rs387906631 | |
pharmgkb | rs387906631 |
gwascentral | rs387906631 |
openSNP | rs387906631 |
23andMe | rs387906631 |
SNPshot | rs387906631 |
SNPdbe | rs387906631 |
MSV3d | rs387906631 |
GWAS Ctlg | rs387906631 |
Max Magnitude | 0 |
aka NM_001145661.1(GATA2):c.1061C>T or (p.Thr354Met)
OMIM pathogenic variant