rs34830032

Orientation

plus

Stabilized

plus

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

Make rs34830032(C;G)

Make rs34830032(G;G)

Reference

GRCh38 38.1/141

Chromosome

16

Position

177319

Gene

HBA1

is a	snp
is	mentioned by
dbSNP	rs34830032
dbSNP (classic)	rs34830032
ClinGen	rs34830032
ebi	rs34830032
HLI	rs34830032
Exac	rs34830032
Gnomad	rs34830032
Varsome	rs34830032
LitVar	rs34830032
Map	rs34830032
PheGenI	rs34830032
Biobank	rs34830032
1000 genomes	rs34830032
hgdp	rs34830032
ensembl	rs34830032
geneview	rs34830032
scholar	rs34830032
google	rs34830032
pharmgkb	rs34830032
gwascentral	rs34830032
openSNP	rs34830032
23andMe	rs34830032
SNPshot	rs34830032
SNPdbe	rs34830032
MSV3d	rs34830032
GWAS Ctlg	rs34830032

Merged from

Rs63749881

Max Magnitude

0

OMIM	141800
Desc
Variant	0054
Related	also

ClinVar
Risk	rs34830032(G;G)
Alt	rs34830032(G;G)
Reference	Rs34830032(C;C)
Significance	Other
Disease	HEMOGLOBIN HOPKINS 2
Variation	info
Gene	HBA1
CLNDBN	HEMOGLOBIN HOPKINS 2
Reversed	0
HGVS	NC_000016.9:g.227318C>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017050.3,

[PMID 646867] The structure of hemoglobin Hopkins-2.

[PMID 5288820] Clinical studies and physiological properties of Hopkins-2 haemoglobin.