rs35661168

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs35661168(A;T)

Make rs35661168(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5234559

Gene

HBD

is a	snp
is	mentioned by
dbSNP	rs35661168
dbSNP (classic)	rs35661168
ClinGen	rs35661168
ebi	rs35661168
HLI	rs35661168
Exac	rs35661168
Gnomad	rs35661168
Varsome	rs35661168
LitVar	rs35661168
Map	rs35661168
PheGenI	rs35661168
Biobank	rs35661168
1000 genomes	rs35661168
hgdp	rs35661168
ensembl	rs35661168
geneview	rs35661168
scholar	rs35661168
google	rs35661168
pharmgkb	rs35661168
gwascentral	rs35661168
openSNP	rs35661168
23andMe	rs35661168
SNPshot	rs35661168
SNPdbe	rs35661168
MSV3d	rs35661168
GWAS Ctlg	rs35661168

Max Magnitude

0

OMIM	142000
Desc
Variant	0044
Related	also

ClinVar
Risk	rs35661168(T;T)
Alt	rs35661168(T;T)
Reference	Rs35661168(A;A)
Significance	Pathogenic
Disease	delta Thalassemia
Variation	info
Gene	HBD
CLNDBN	delta Thalassemia
Reversed	1
HGVS	NC_000011.9:g.5255789T>A
CLNSRC	HBVAR OMIM Allelic Variant
CLNACC	RCV000016238.25,

[PMID 12402333] Epidemiology of the delta globin alleles in southern Italy shows complex molecular, genetic, and phenotypic features.