rs28928882

Orientation

plus

Stabilized

plus

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

Make rs28928882(A;A)

Make rs28928882(A;C)

Reference

GRCh38 38.1/141

Chromosome

16

Position

173248

Gene

HBA2

is a	snp
is	mentioned by
dbSNP	rs28928882
dbSNP (classic)	rs28928882
ClinGen	rs28928882
ebi	rs28928882
HLI	rs28928882
Exac	rs28928882
Gnomad	rs28928882
Varsome	rs28928882
LitVar	rs28928882
Map	rs28928882
PheGenI	rs28928882
Biobank	rs28928882
1000 genomes	rs28928882
hgdp	rs28928882
ensembl	rs28928882
geneview	rs28928882
scholar	rs28928882
google	rs28928882
pharmgkb	rs28928882
gwascentral	rs28928882
openSNP	rs28928882
23andMe	rs28928882
SNPshot	rs28928882
SNPdbe	rs28928882
MSV3d	rs28928882
GWAS Ctlg	rs28928882

Max Magnitude

0

OMIM	141800
Desc	HEMOGLOBIN GOUDA
Variant	0198
Related	also

ClinVar
Risk	rs28928882(A;A)
Alt	rs28928882(A;A)
Reference	Rs28928882(C;C)
Significance	Other
Disease	HEMOGLOBIN GOUDA
Variation	info
Gene	HBA2
CLNDBN	HEMOGLOBIN GOUDA
Reversed	0
HGVS	NC_000016.9:g.223247C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000017217.1,

[PMID 8745429] HB Gouda [alpha 72(EF1)His-->Gln], a new silent alpha chain variant.