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rs397509430

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397509430(-;-)
Make rs397509430(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position5227101
GeneHBB
is asnp
is mentioned by
dbSNPrs397509430
ebirs397509430
HLIrs397509430
Exacrs397509430
Varsomers397509430
Maprs397509430
PheGenIrs397509430
hapmaprs397509430
1000 genomesrs397509430
hgdprs397509430
ensemblrs397509430
gopubmedrs397509430
geneviewrs397509430
scholarrs397509430
googlers397509430
pharmgkbrs397509430
gwascentralrs397509430
openSNPrs397509430
23andMers397509430
23andMe allrs397509430
SNP Nexus

SNPshotrs397509430
SNPdbers397509430
MSV3drs397509430
GWAS Ctlgrs397509430
Max Magnitude0

[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,