rs34743882

Orientation

minus

Stabilized

minus

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

Make rs34743882(A;A)

Make rs34743882(A;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5226753

Gene

HBB

is a	snp
is	mentioned by
dbSNP	rs34743882
dbSNP (classic)	rs34743882
ClinGen	rs34743882
ebi	rs34743882
HLI	rs34743882
Exac	rs34743882
Gnomad	rs34743882
Varsome	rs34743882
LitVar	rs34743882
Map	rs34743882
PheGenI	rs34743882
Biobank	rs34743882
1000 genomes	rs34743882
hgdp	rs34743882
ensembl	rs34743882
geneview	rs34743882
scholar	rs34743882
google	rs34743882
pharmgkb	rs34743882
gwascentral	rs34743882
openSNP	rs34743882
23andMe	rs34743882
SNPshot	rs34743882
SNPdbe	rs34743882
MSV3d	rs34743882
GWAS Ctlg	rs34743882

Max Magnitude

0

OMIM	141900
Desc
Variant	0090
Related	also

ClinVar
Risk	rs34743882(A;A)
Alt	rs34743882(A;A)
Reference	Rs34743882(G;G)
Significance	Other
Disease	HEMOGLOBIN GAINESVILLE-GA
Variation	info
Gene	HBB
CLNDBN	HEMOGLOBIN GAINESVILLE-GA
Reversed	1
HGVS	NC_000011.9:g.5247983C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000016358.3,

[PMID 2481659] Hb Gainesville-GA or alpha 2 beta 2(46)(CD5)Gly----Arg; second report.

[PMID 3839773] Hb Gainesville-GA or alpha 2 beta 2 46(CD5)Gly----Arg.