rs28928885

Orientation

plus

Stabilized

plus

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

Make rs28928885(C;G)

Make rs28928885(G;G)

Reference

GRCh38 38.1/141

Chromosome

16

Position

176746

Gene

HBA1

is a	snp
is	mentioned by
dbSNP	rs28928885
dbSNP (classic)	rs28928885
ClinGen	rs28928885
ebi	rs28928885
HLI	rs28928885
Exac	rs28928885
Gnomad	rs28928885
Varsome	rs28928885
LitVar	rs28928885
Map	rs28928885
PheGenI	rs28928885
Biobank	rs28928885
1000 genomes	rs28928885
hgdp	rs28928885
ensembl	rs28928885
geneview	rs28928885
scholar	rs28928885
google	rs28928885
pharmgkb	rs28928885
gwascentral	rs28928885
openSNP	rs28928885
23andMe	rs28928885
SNPshot	rs28928885
SNPdbe	rs28928885
MSV3d	rs28928885
GWAS Ctlg	rs28928885

Max Magnitude

0

OMIM	141800
Desc	HEMOGLOBIN DELFZICHT
Variant	0208
Related	also

OMIM	141850
Desc
Variant	0048
Related	also

ClinVar
Risk	rs28928885(G;G)
Alt	rs28928885(G;G)
Reference	Rs28928885(C;C)
Significance	Other
Disease	HEMOGLOBIN DELFZICHT
Variation	info
Gene	HBA1
CLNDBN	HEMOGLOBIN DELFZICHT
Reversed	0
HGVS	NC_000016.9:g.226745C>G
CLNSRC	HBVAR OMIM Allelic Variant
CLNACC	RCV000017227.2,

[PMID 12144062] Hb delfzicht [alpha9(A7)Asn-->Lys (alpha1)]: a new, clinically silent hemoglobin variant observed in a Dutch patient.