rs111645889

Orientation

minus

Stabilized

minus

Make rs111645889(C;C)

Make rs111645889(C;T)

Make rs111645889(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5225653

Gene

HBB

is a	snp
is	mentioned by
dbSNP	rs111645889
dbSNP (classic)	rs111645889
ClinGen	rs111645889
ebi	rs111645889
HLI	rs111645889
Exac	rs111645889
Gnomad	rs111645889
Varsome	rs111645889
LitVar	rs111645889
Map	rs111645889
PheGenI	rs111645889
Biobank	rs111645889
1000 genomes	rs111645889
hgdp	rs111645889
ensembl	rs111645889
geneview	rs111645889
scholar	rs111645889
google	rs111645889
pharmgkb	rs111645889
gwascentral	rs111645889
openSNP	rs111645889
23andMe	rs111645889
SNPshot	rs111645889
SNPdbe	rs111645889
MSV3d	rs111645889
GWAS Ctlg	rs111645889

Merged from

Rs33942582

GMAF

0.0004591

Max Magnitude

0

OMIM	141900
Desc
Variant	0138
Related	also

OMIM	141900
Desc
Variant	0154
Related	also

ClinVar
Risk	rs111645889(A;A) rs111645889(T;T)
Alt	rs111645889(A;A) rs111645889(T;T)
Reference	rs111645889(C;C)
Significance	Other
Disease	HEMOGLOBIN LA DESIRADE HEMOGLOBIN J (TAICHUNG) HEMOGLOBIN K (CAMEROON)
Variation	info
Gene	HBB
CLNDBN	HEMOGLOBIN LA DESIRADE HEMOGLOBIN J (TAICHUNG) HEMOGLOBIN K (CAMEROON)
Reversed	1
HGVS	NC_000011.9:g.5246883G>A; NC_000011.9:g.5246883G>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000016450.2, RCV000016426.2, RCV000016429.2,

[PMID 5353125] Hemoglobin J Taichung:beta-129 ALA--ASP.

[PMID 3557994] Hemoglobin La Desirade alpha A2 beta 2 129 (H7) Ala----Val: a new unstable hemoglobin.