rs33942582

Merged into

rs111645889

Orientation

minus

Stabilized

minus

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

Make rs33942582(A;A)

Make rs33942582(A;C)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5225653

Gene

HBB

is a	snp
is	mentioned by
dbSNP	rs33942582
dbSNP (classic)	rs33942582
ClinGen	rs33942582
ebi	rs33942582
HLI	rs33942582
Exac	rs33942582
Gnomad	rs33942582
Varsome	rs33942582
LitVar	rs33942582
Map	rs33942582
PheGenI	rs33942582
Biobank	rs33942582
1000 genomes	rs33942582
hgdp	rs33942582
ensembl	rs33942582
geneview	rs33942582
scholar	rs33942582
google	rs33942582
pharmgkb	rs33942582
gwascentral	rs33942582
openSNP	rs33942582
23andMe	rs33942582
SNPshot	rs33942582
SNPdbe	rs33942582
MSV3d	rs33942582
GWAS Ctlg	rs33942582

Status

Merged into rs111645889

Max Magnitude

0

OMIM	141900
Desc
Variant	0138
Related	also

OMIM	141900
Desc
Variant	0154
Related	also

ClinVar
Risk	rs33942582(AAC;AAC) rs33942582(AC;AC) rs33942582(ACC;ACC) rs33942582(CCC;CCC) rs33942582(TC;TC)
Alt	rs33942582(AAC;AAC) rs33942582(AC;AC) rs33942582(ACC;ACC) rs33942582(CCC;CCC) rs33942582(TC;TC)
Reference	Rs33942582(CC;CC)
Significance	Untested
Disease
Variation	info
Gene	HBB
CLNDBN
Reversed	1
HGVS	NC_000011.9:g.5246883G>A; NC_000011.9:g.5246883G>T
CLNSRC
CLNACC