rs28933076

Orientation

minus

Stabilized

minus

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

Make rs28933076(A;A)

Make rs28933076(A;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5234011

Gene

HBD

is a	snp
is	mentioned by
dbSNP	rs28933076
dbSNP (classic)	rs28933076
ClinGen	rs28933076
ebi	rs28933076
HLI	rs28933076
Exac	rs28933076
Gnomad	rs28933076
Varsome	rs28933076
LitVar	rs28933076
Map	rs28933076
PheGenI	rs28933076
Biobank	rs28933076
1000 genomes	rs28933076
hgdp	rs28933076
ensembl	rs28933076
geneview	rs28933076
scholar	rs28933076
google	rs28933076
pharmgkb	rs28933076
gwascentral	rs28933076
openSNP	rs28933076
23andMe	rs28933076
SNPshot	rs28933076
SNPdbe	rs28933076
MSV3d	rs28933076
GWAS Ctlg	rs28933076

Max Magnitude

0

OMIM	142000
Desc	HEMOGLOBIN A(2) WRENS
Variant	0016
Related	also

ClinVar
Risk	rs28933076(A;A)
Alt	rs28933076(A;A)
Reference	Rs28933076(G;G)
Significance	Other
Disease	HEMOGLOBIN A(2) WRENS
Variation	info
Gene	HBD
CLNDBN	HEMOGLOBIN A(2) WRENS
Reversed	1
HGVS	NC_000011.9:g.5255241C>T
CLNSRC	HBVAR OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000016204.1,

[PMID 2477064] Hb A2-Wrens or alpha 2 delta 2 98(FG5) Val----Met, an unstable delta chain variant identified by sequence analysis of amplified DNA.