rs397509430

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
google	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,