rs397509430
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs397509430(-;-) |
Make rs397509430(-;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 11 |
Position | 5227101 |
Gene | HBB |
is a | snp |
is | mentioned by |
dbSNP | rs397509430 |
dbSNP (classic) | rs397509430 |
ClinGen | rs397509430 |
ebi | rs397509430 |
HLI | rs397509430 |
Exac | rs397509430 |
Gnomad | rs397509430 |
Varsome | rs397509430 |
LitVar | rs397509430 |
Map | rs397509430 |
PheGenI | rs397509430 |
Biobank | rs397509430 |
1000 genomes | rs397509430 |
hgdp | rs397509430 |
ensembl | rs397509430 |
geneview | rs397509430 |
scholar | rs397509430 |
rs397509430 | |
pharmgkb | rs397509430 |
gwascentral | rs397509430 |
openSNP | rs397509430 |
23andMe | rs397509430 |
SNPshot | rs397509430 |
SNPdbe | rs397509430 |
MSV3d | rs397509430 |
GWAS Ctlg | rs397509430 |
Max Magnitude | 0 |
[PMID 26694100] Obesity-related known and candidate SNP markers can significantly change affinity of TATA-binding protein for human gene promoters.
ClinVar | |
---|---|
Risk | rs397509430(-;-) |
Alt | rs397509430(-;-) |
Reference | Rs397509430(T;T) |
Significance | Untested |
Disease | Beta Thalassemia |
Variation | info |
Gene | HBB |
CLNDBN | beta Thalassemia |
Reversed | 1 |
HGVS | NC_000011.9:g.5248331delA |
CLNSRC | |
CLNACC | RCV000054503.1, |