rs33928092

Orientation

minus

Stabilized

minus

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

Make rs33928092(A;A)

Make rs33928092(A;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5225686

Gene

HBB

is a	snp
is	mentioned by
dbSNP	rs33928092
dbSNP (classic)	rs33928092
ClinGen	rs33928092
ebi	rs33928092
HLI	rs33928092
Exac	rs33928092
Gnomad	rs33928092
Varsome	rs33928092
LitVar	rs33928092
Map	rs33928092
PheGenI	rs33928092
Biobank	rs33928092
1000 genomes	rs33928092
hgdp	rs33928092
ensembl	rs33928092
geneview	rs33928092
scholar	rs33928092
google	rs33928092
pharmgkb	rs33928092
gwascentral	rs33928092
openSNP	rs33928092
23andMe	rs33928092
SNPshot	rs33928092
SNPdbe	rs33928092
MSV3d	rs33928092
GWAS Ctlg	rs33928092

Max Magnitude

0

OMIM	141900
Desc
Variant	0176
Related	also

OMIM	141900
Desc
Variant	0486
Related	also

ClinVar
Risk	rs33928092(A;A) rs33928092(C;C) rs33928092(G;G)
Alt	rs33928092(A;A) rs33928092(C;C) rs33928092(G;G)
Reference	Rs33928092(T;T)
Significance	Other
Disease	HEMOGLOBIN HARROW HEMOGLOBIN MINNEAPOLIS-LAOS
Variation	info
Gene	HBB
CLNDBN	HEMOGLOBIN HARROW HEMOGLOBIN MINNEAPOLIS-LAOS
Reversed	1
HGVS	NC_000011.9:g.5246916A>C; NC_000011.9:g.5246916A>T
CLNSRC	HBVAR OMIM Allelic Variant
CLNACC	RCV000016841.2, RCV000016490.2,

[PMID 3667327] A second family with Hb Minneapolis-Laos or alpha 2 beta (2)118(GH1)Phe----Tyr.

[PMID 6547119] Hemoglobin Minneapolis-Laos [beta-118 (GH1) Phe----Tyr] A new hemoglobin variant with normal functional properties.

[PMID 10490141] Hb Harrow [beta118(GH1)Phe-->Cys]: a new neutral hemoglobin variant.