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rs33910475

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs33910475(A;G)
Make rs33910475(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position5225624
GeneHBB
is asnp
is mentioned by
dbSNPrs33910475
ebirs33910475
HLIrs33910475
Exacrs33910475
Varsomers33910475
Maprs33910475
PheGenIrs33910475
hapmaprs33910475
1000 genomesrs33910475
hgdprs33910475
ensemblrs33910475
gopubmedrs33910475
geneviewrs33910475
scholarrs33910475
googlers33910475
pharmgkbrs33910475
gwascentralrs33910475
openSNPrs33910475
23andMers33910475
23andMe allrs33910475
SNP Nexus

SNPshotrs33910475
SNPdbers33910475
MSV3drs33910475
GWAS Ctlgrs33910475
Max Magnitude0
OMIM141900
Desc
Variant0092
Relatedalso
OMIM141900
Desc
Variant0459
Relatedalso
ClinVar
Risk rs33910475(G,T;G,T)
Alt rs33910475(G,T;G,T)
Reference rs33910475(A;A)
Significance Other
Disease HEMOGLOBIN AURORA HEMOGLOBIN GEELONG HEMOGLOBIN JINAN
Variation info
Gene HBB
CLNDBN HEMOGLOBIN AURORA HEMOGLOBIN GEELONG HEMOGLOBIN JINAN
Reversed 1
HGVS NC_000011.9:g.5246854T>A; NC_000011.9:g.5246854T>C
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000016813.2, RCV000016360.3, RCV000016361.3,


[PMID 1917539] Hb Geelong [beta 139(H17)Asn----Asp].


[PMID 8718692] Identification of a new high oxygen affinity hemoglobin variant: Hb Aurora [beta 139(H17) Asn-->Tyr].