rs33930476

Merged into

rs281864894

Orientation

minus

Stabilized

minus

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

Make rs33930476(C;T)

Make rs33930476(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5226738

Gene

HBB

is a	snp
is	mentioned by
dbSNP	rs33930476
dbSNP (classic)	rs33930476
ClinGen	rs33930476
ebi	rs33930476
HLI	rs33930476
Exac	rs33930476
Gnomad	rs33930476
Varsome	rs33930476
LitVar	rs33930476
Map	rs33930476
PheGenI	rs33930476
Biobank	rs33930476
1000 genomes	rs33930476
hgdp	rs33930476
ensembl	rs33930476
geneview	rs33930476
scholar	rs33930476
google	rs33930476
pharmgkb	rs33930476
gwascentral	rs33930476
openSNP	rs33930476
23andMe	rs33930476
SNPshot	rs33930476
SNPdbe	rs33930476
MSV3d	rs33930476
GWAS Ctlg	rs33930476

Status

Merged into rs281864894

Max Magnitude

0

OMIM	141900
Desc
Variant	0408
Related	also

ClinVar
Risk	rs33930476(TC;TC) Rs33930476(C;C)
Alt	rs33930476(TC;TC) Rs33930476(C;C)
Reference	Rs33930476(CC;CC)
Significance	Untested
Disease
Variation	info
Gene	HBB
CLNDBN
Reversed	1
HGVS	NC_000011.9:g.5247968G>A
CLNSRC
CLNACC