rs34460332

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in complete genomics

Make rs34460332(A;A)

Make rs34460332(A;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5234360

Gene

HBD

is a	snp
is	mentioned by
dbSNP	rs34460332
dbSNP (classic)	rs34460332
ClinGen	rs34460332
ebi	rs34460332
HLI	rs34460332
Exac	rs34460332
Gnomad	rs34460332
Varsome	rs34460332
LitVar	rs34460332
Map	rs34460332
PheGenI	rs34460332
Biobank	rs34460332
1000 genomes	rs34460332
hgdp	rs34460332
ensembl	rs34460332
geneview	rs34460332
scholar	rs34460332
google	rs34460332
pharmgkb	rs34460332
gwascentral	rs34460332
openSNP	rs34460332
23andMe	rs34460332
SNPshot	rs34460332
SNPdbe	rs34460332
MSV3d	rs34460332
GWAS Ctlg	rs34460332

Max Magnitude

0

OMIM	142000
Desc
Variant	0015
Related	also

?	(A;G) (G;G)

ClinVar
Risk	rs34460332(A;A)
Alt	rs34460332(A;A)
Reference	Rs34460332(G;G)
Significance	Other
Disease	HEMOGLOBIN A(2) VICTORIA
Variation	info
Gene	HBD
CLNDBN	HEMOGLOBIN A(2) VICTORIA
Reversed	1
HGVS	NC_000011.9:g.5255590C>T
CLNSRC	HBVAR OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000016203.1,

[PMID 6469695] HbA2 Victoria delta 24 (B6) Gly----Asp. A new delta chain variant occurring with beta-thalassemia.