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rs33948057

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs33948057(A;G)
Make rs33948057(G;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position5226584
GeneHBB
is asnp
is mentioned by
dbSNPrs33948057
ebirs33948057
HLIrs33948057
Exacrs33948057
Varsomers33948057
Maprs33948057
PheGenIrs33948057
hapmaprs33948057
1000 genomesrs33948057
hgdprs33948057
ensemblrs33948057
gopubmedrs33948057
geneviewrs33948057
scholarrs33948057
googlers33948057
pharmgkbrs33948057
gwascentralrs33948057
openSNPrs33948057
23andMers33948057
23andMe allrs33948057
SNP Nexus

SNPshotrs33948057
SNPdbers33948057
MSV3drs33948057
GWAS Ctlgrs33948057
Max Magnitude0
OMIM141900
Desc
Variant0021
Relatedalso
OMIM141900
Desc
Variant0145
Relatedalso


ClinVar
Risk rs33948057(C,G;C,G)
Alt rs33948057(C,G;C,G)
Reference rs33948057(A;A)
Significance Other
Disease HEMOGLOBIN BETH ISRAEL not specified
Variation info
Gene HBB
CLNDBN HEMOGLOBIN BETH ISRAEL not specified
Reversed 1
HGVS NC_000011.9:g.5247814T>C; NC_000011.9:g.5247814T>G
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000016266.2, RCV000016434.3,



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[PMID 7451490] Conformational studies of hemoglobins using intrinsic fluorescence measurements.