rs33999427

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
({{{allele1}}};{{{allele2}}})	0	common in clinvar
(-;-)	0	common in complete genomics
(T;T)	0	common in clinvar

Make rs33999427(-;AC)

Make rs33999427(AC;AC)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5225600

Gene

HBB

is a	snp
is	mentioned by
dbSNP	rs33999427
dbSNP (classic)	rs33999427
ClinGen	rs33999427
ebi	rs33999427
HLI	rs33999427
Exac	rs33999427
Gnomad	rs33999427
Varsome	rs33999427
LitVar	rs33999427
Map	rs33999427
PheGenI	rs33999427
Biobank	rs33999427
1000 genomes	rs33999427
hgdp	rs33999427
ensembl	rs33999427
geneview	rs33999427
scholar	rs33999427
google	rs33999427
pharmgkb	rs33999427
gwascentral	rs33999427
openSNP	rs33999427
23andMe	rs33999427
SNPshot	rs33999427
SNPdbe	rs33999427
MSV3d	rs33999427
GWAS Ctlg	rs33999427

Max Magnitude

0

OMIM	141900
Desc
Variant	0279
Related	also

ClinVar
Risk	rs33999427(TAT;TAT) rs33999427(ACT;ACT)
Alt	rs33999427(TAT;TAT) rs33999427(ACT;ACT)
Reference	Rs33999427(T;T)
Significance	Untested
Disease
Variation	info
Gene	HBB
CLNDBN
Reversed	1
HGVS	NC_000011.9:g.5246830_5246831insGT; NC_000011.9:g.5246830_5246831insTA
CLNSRC
CLNACC

[PMID 88] The oxygen affinity of haemoglobin Tak, a variant with an elongated beta chain.