rs33976776

Orientation

plus

Stabilized

plus

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

Make rs33976776(A;G)

Make rs33976776(G;G)

Reference

GRCh38 38.1/141

Chromosome

16

Position

177096

Gene

HBA1

is a	snp
is	mentioned by
dbSNP	rs33976776
dbSNP (classic)	rs33976776
ClinGen	rs33976776
ebi	rs33976776
HLI	rs33976776
Exac	rs33976776
Gnomad	rs33976776
Varsome	rs33976776
LitVar	rs33976776
Map	rs33976776
PheGenI	rs33976776
Biobank	rs33976776
1000 genomes	rs33976776
hgdp	rs33976776
ensembl	rs33976776
geneview	rs33976776
scholar	rs33976776
google	rs33976776
pharmgkb	rs33976776
gwascentral	rs33976776
openSNP	rs33976776
23andMe	rs33976776
SNPshot	rs33976776
SNPdbe	rs33976776
MSV3d	rs33976776
GWAS Ctlg	rs33976776

Max Magnitude

0

OMIM	141800
Desc
Variant	0057
Related	also

ClinVar
Risk	rs33976776(C;C) rs33976776(G;G)
Alt	rs33976776(C;C) rs33976776(G;G)
Reference	Rs33976776(A;A)
Significance	Other
Disease	HEMOGLOBIN IWATA
Variation	info
Gene	HBA1
CLNDBN	HEMOGLOBIN IWATA
Reversed	0
HGVS	NC_000016.9:g.227095A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017056.2,

[PMID 6874376] A case of hemoglobin Iwata [alpha 87(F8)His leads to Arg] in China.

[PMID 7419426] Unstable hemoglobins in Japan.