rs33931984

Orientation

plus

Stabilized

plus

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

Make rs33931984(C;G)

Make rs33931984(G;G)

Reference

GRCh38 38.1/141

Chromosome

16

Position

176969

Gene

HBA1

is a	snp
is	mentioned by
dbSNP	rs33931984
dbSNP (classic)	rs33931984
ClinGen	rs33931984
ebi	rs33931984
HLI	rs33931984
Exac	rs33931984
Gnomad	rs33931984
Varsome	rs33931984
LitVar	rs33931984
Map	rs33931984
PheGenI	rs33931984
Biobank	rs33931984
1000 genomes	rs33931984
hgdp	rs33931984
ensembl	rs33931984
geneview	rs33931984
scholar	rs33931984
google	rs33931984
pharmgkb	rs33931984
gwascentral	rs33931984
openSNP	rs33931984
23andMe	rs33931984
SNPshot	rs33931984
SNPdbe	rs33931984
MSV3d	rs33931984
GWAS Ctlg	rs33931984

Max Magnitude

0

OMIM	141800
Desc
Variant	0176
Related	also

ClinVar
Risk	rs33931984(G;G) rs33931984(T;T)
Alt	rs33931984(G;G) rs33931984(T;T)
Reference	Rs33931984(C;C)
Significance	Other
Disease	HEMOGLOBIN POITIERS
Variation	info
Gene	HBA1
CLNDBN	HEMOGLOBIN POITIERS
Reversed	0
HGVS	NC_000016.9:g.226968C>G
CLNSRC	HBVAR OMIM Allelic Variant
CLNACC	RCV000017196.2,

[PMID 8195004] Hb Poitiers [alpha 45(CE3)His-->Asp]: a new hemoglobin variant with a two-fold increase in oxygen affinity.