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rs33967755

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs33967755(A;T)
Make rs33967755(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position5226671
GeneHBB
is asnp
is mentioned by
dbSNPrs33967755
ebirs33967755
HLIrs33967755
Exacrs33967755
Varsomers33967755
Maprs33967755
PheGenIrs33967755
hapmaprs33967755
1000 genomesrs33967755
hgdprs33967755
ensemblrs33967755
gopubmedrs33967755
geneviewrs33967755
scholarrs33967755
googlers33967755
pharmgkbrs33967755
gwascentralrs33967755
openSNPrs33967755
23andMers33967755
23andMe allrs33967755
SNP Nexus

SNPshotrs33967755
SNPdbers33967755
MSV3drs33967755
GWAS Ctlgrs33967755
Max Magnitude0
OMIM141900
Desc
Variant0183
Relatedalso
OMIM141900
Desc
Variant0283
Relatedalso
ClinVar
Risk rs33967755(G,T;G,T)
Alt rs33967755(G,T;G,T)
Reference rs33967755(A;A)
Significance Other
Disease HEMOGLOBIN MOBILE HEMOGLOBIN TILBURG
Variation info
Gene HBB
CLNDBN HEMOGLOBIN MOBILE HEMOGLOBIN TILBURG
Reversed 1
HGVS NC_000011.9:g.5247901T>A; NC_000011.9:g.5247901T>C
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000016499.2, RCV000016625.2,


[PMID 1018330] Hemoglobin Vancouver [alpha2beta2(73)(E17) Asp replaced by Tyr]: its structure and function.


[PMID 1180880] Hb Mobile [alpha2beta2 73(E17)Asp replaced by Val]: a new variant.


[PMID 3191145] Hemoglobin Tilburg: alpha 2-beta 2 73 (E 17) Asp----Gly. A new hemoglobin with reduced oxygen affinity.