rs33946775

Orientation

minus

Stabilized

minus

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

Make rs33946775(A;C)

Make rs33946775(C;C)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5225643

Gene

HBB

is a	snp
is	mentioned by
dbSNP	rs33946775
dbSNP (classic)	rs33946775
ClinGen	rs33946775
ebi	rs33946775
HLI	rs33946775
Exac	rs33946775
Gnomad	rs33946775
Varsome	rs33946775
LitVar	rs33946775
Map	rs33946775
PheGenI	rs33946775
Biobank	rs33946775
1000 genomes	rs33946775
hgdp	rs33946775
ensembl	rs33946775
geneview	rs33946775
scholar	rs33946775
google	rs33946775
pharmgkb	rs33946775
gwascentral	rs33946775
openSNP	rs33946775
23andMe	rs33946775
SNPshot	rs33946775
SNPdbe	rs33946775
MSV3d	rs33946775
GWAS Ctlg	rs33946775

Max Magnitude

0

OMIM	141900
Desc
Variant	0302
Related	also

ClinVar
Risk	rs33946775(C;C) rs33946775(T;T)
Alt	rs33946775(C;C) rs33946775(T;T)
Reference	Rs33946775(A;A)
Significance	Untested
Disease
Variation	info
Gene	HBB
CLNDBN
Reversed	1
HGVS	NC_000011.9:g.5246873T>A; NC_000011.9:g.5246873T>G
CLNSRC
CLNACC

[PMID 2272843] Hb Yamagata [beta 132(H10)Lys----Asn]: a new abnormal hemoglobin in a Japanese family.

[PMID 8811322] A new observation of Hb Yamagata with a different nucleotide substitution: beta 132 AAA-->AAT.