rs33961459

Orientation

minus

Stabilized

minus

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

Make rs33961459(C;T)

Make rs33961459(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5226687

Gene

HBB

is a	snp
is	mentioned by
dbSNP	rs33961459
dbSNP (classic)	rs33961459
ClinGen	rs33961459
ebi	rs33961459
HLI	rs33961459
Exac	rs33961459
Gnomad	rs33961459
Varsome	rs33961459
LitVar	rs33961459
Map	rs33961459
PheGenI	rs33961459
Biobank	rs33961459
1000 genomes	rs33961459
hgdp	rs33961459
ensembl	rs33961459
geneview	rs33961459
scholar	rs33961459
google	rs33961459
pharmgkb	rs33961459
gwascentral	rs33961459
openSNP	rs33961459
23andMe	rs33961459
SNPshot	rs33961459
SNPdbe	rs33961459
MSV3d	rs33961459
GWAS Ctlg	rs33961459

Max Magnitude

0

OMIM	141900
Desc
Variant	0523
Related	also

OMIM	141900
Desc
Variant	0524
Related	also

ClinVar
Risk	rs33961459(T;T)
Alt	rs33961459(T;T)
Reference	Rs33961459(C;C)
Significance	Other
Disease	HEMOGLOBIN JAMAICA PLAIN HEMOGLOBIN ROCKFORD
Variation	info
Gene	HBB
CLNDBN	HEMOGLOBIN JAMAICA PLAIN HEMOGLOBIN ROCKFORD
Reversed	1
HGVS	NC_000011.9:g.5247917G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000016879.3, RCV000016880.2,

[PMID 16550507] Hemoglobin Loves Park [beta68 (E12) Leu-->Phe]: report of five cases including one originating from a de novo mutation.