rs34665886

Orientation

minus

Stabilized

minus

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

Make rs34665886(C;G)

Make rs34665886(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5226603

Gene

HBB

is a	snp
is	mentioned by
dbSNP	rs34665886
dbSNP (classic)	rs34665886
ClinGen	rs34665886
ebi	rs34665886
HLI	rs34665886
Exac	rs34665886
Gnomad	rs34665886
Varsome	rs34665886
LitVar	rs34665886
Map	rs34665886
PheGenI	rs34665886
Biobank	rs34665886
1000 genomes	rs34665886
hgdp	rs34665886
ensembl	rs34665886
geneview	rs34665886
scholar	rs34665886
google	rs34665886
pharmgkb	rs34665886
gwascentral	rs34665886
openSNP	rs34665886
23andMe	rs34665886
SNPshot	rs34665886
SNPdbe	rs34665886
MSV3d	rs34665886
GWAS Ctlg	rs34665886

Max Magnitude

0

OMIM	141900
Desc
Variant	0235
Related	also

ClinVar
Risk	rs34665886(G;G)
Alt	rs34665886(G;G)
Reference	Rs34665886(C;C)
Significance	Other
Disease	HEMOGLOBIN REGINA
Variation	info
Gene	HBB
CLNDBN	HEMOGLOBIN REGINA
Reversed	1
HGVS	NC_000011.9:g.5247833G>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000016565.3,

[PMID 3839106] Hb Regina or alpha 2 beta 2 96(FG3)Leu----Val: a high oxygen affinity variant discovered by cation-exchange HPLC.