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rs33942582

From SNPedia

Merged intors111645889
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
(CC;CC) 0 common in clinvar
Make rs33942582(A;A)
Make rs33942582(A;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position5225653
GeneHBB
is asnp
is mentioned by
dbSNPrs33942582
ebirs33942582
HLIrs33942582
Exacrs33942582
Varsomers33942582
Maprs33942582
PheGenIrs33942582
hapmaprs33942582
1000 genomesrs33942582
hgdprs33942582
ensemblrs33942582
gopubmedrs33942582
geneviewrs33942582
scholarrs33942582
googlers33942582
pharmgkbrs33942582
gwascentralrs33942582
openSNPrs33942582
23andMers33942582
23andMe allrs33942582
SNP Nexus

SNPshotrs33942582
SNPdbers33942582
MSV3drs33942582
GWAS Ctlgrs33942582
StatusMerged into rs111645889
Max Magnitude0
OMIM141900
Desc
Variant0138
Relatedalso
OMIM141900
Desc
Variant0154
Relatedalso
ClinVar
Risk rs33942582(AAC,AC,ACC,CCC,TC;AAC,AC,ACC,CCC,TC)
Alt rs33942582(AAC,AC,ACC,CCC,TC;AAC,AC,ACC,CCC,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