rs33926764

Orientation

minus

Stabilized

minus

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

Make rs33926764(A;C)

Make rs33926764(C;C)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5226997

Gene

HBB

is a	snp
is	mentioned by
dbSNP	rs33926764
dbSNP (classic)	rs33926764
ClinGen	rs33926764
ebi	rs33926764
HLI	rs33926764
Exac	rs33926764
Gnomad	rs33926764
Varsome	rs33926764
LitVar	rs33926764
Map	rs33926764
PheGenI	rs33926764
Biobank	rs33926764
1000 genomes	rs33926764
hgdp	rs33926764
ensembl	rs33926764
geneview	rs33926764
scholar	rs33926764
google	rs33926764
pharmgkb	rs33926764
gwascentral	rs33926764
openSNP	rs33926764
23andMe	rs33926764
SNPshot	rs33926764
SNPdbe	rs33926764
MSV3d	rs33926764
GWAS Ctlg	rs33926764

Max Magnitude

0

OMIM	141900
Desc
Variant	0135
Related	also

OMIM	141900
Desc
Variant	0191
Related	also

ClinVar
Risk	rs33926764(C;C) rs33926764(G;G)
Alt	rs33926764(C;C) rs33926764(G;G)
Reference	Rs33926764(A;A)
Significance	Other
Disease	HEMOGLOBIN N (TIMONE) HEMOGLOBIN J (LUHE)
Variation	info
Gene	HBB
CLNDBN	HEMOGLOBIN N (TIMONE) HEMOGLOBIN J (LUHE)
Reversed	1
HGVS	NC_000011.9:g.5248227T>C; NC_000011.9:g.5248227T>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein) HBVAR
CLNACC	RCV000016511.2, RCV000016422.3,

[PMID 2634671] Hb N-Timone [alpha 2 beta 2(8)(A5)Lys----Glu]: a new fast-moving variant with normal stability and oxygen affinity.