rs33943087

Orientation

plus

Stabilized

plus

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

Make rs33943087(A;G)

Make rs33943087(G;G)

Reference

GRCh38 38.1/141

Chromosome

16

Position

176778

Gene

HBA1

is a	snp
is	mentioned by
dbSNP	rs33943087
dbSNP (classic)	rs33943087
ClinGen	rs33943087
ebi	rs33943087
HLI	rs33943087
Exac	rs33943087
Gnomad	rs33943087
Varsome	rs33943087
LitVar	rs33943087
Map	rs33943087
PheGenI	rs33943087
Biobank	rs33943087
1000 genomes	rs33943087
hgdp	rs33943087
ensembl	rs33943087
geneview	rs33943087
scholar	rs33943087
google	rs33943087
pharmgkb	rs33943087
gwascentral	rs33943087
openSNP	rs33943087
23andMe	rs33943087
SNPshot	rs33943087
SNPdbe	rs33943087
MSV3d	rs33943087
GWAS Ctlg	rs33943087

Max Magnitude

0

OMIM	141800
Desc
Variant	0053
Related	also

ClinVar
Risk	rs33943087(C;C) rs33943087(G;G)
Alt	rs33943087(C;C) rs33943087(G;G)
Reference	Rs33943087(A;A)
Significance	Other
Disease	HEMOGLOBIN HOBART
Variation	info
Gene	HBA1
CLNDBN	HEMOGLOBIN HOBART
Reversed	0
HGVS	NC_000016.9:g.226777A>G
CLNSRC	HBVAR OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017049.2,

[PMID 3654264] Hemoglobin Hobart or alpha 20(Bl)His----Arg: a new alpha chain hemoglobin variant.

[PMID 11186259] Hb Anderlecht [alpha20(B1)His-->Pro]: a silent variant found in a Congolese newborn.