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rs33961916

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs33961916(A;A)
Make rs33961916(A;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position176735
GeneHBA1
is asnp
is mentioned by
dbSNPrs33961916
ebirs33961916
HLIrs33961916
Exacrs33961916
Varsomers33961916
Maprs33961916
PheGenIrs33961916
hapmaprs33961916
1000 genomesrs33961916
hgdprs33961916
ensemblrs33961916
gopubmedrs33961916
geneviewrs33961916
scholarrs33961916
googlers33961916
pharmgkbrs33961916
gwascentralrs33961916
openSNPrs33961916
23andMers33961916
23andMe allrs33961916
SNP Nexus

SNPshotrs33961916
SNPdbers33961916
MSV3drs33961916
GWAS Ctlgrs33961916
Max Magnitude0
OMIM141800
Desc
Variant0029
Relatedalso
OMIM141800
Desc
Variant0158
Relatedalso
ClinVar
Risk rs33961916(A,C,T;A,C,T)
Alt rs33961916(A,C,T;A,C,T)
Reference rs33961916(G;G)
Significance Other
Disease HEMOGLOBIN DUNN HEMOGLOBIN WOODVILLE
Variation info
Gene HBA1
CLNDBN HEMOGLOBIN DUNN HEMOGLOBIN WOODVILLE
Reversed 0
HGVS NC_000016.9:g.226734G>A; NC_000016.9:g.226734G>T
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000017016.2, RCV000017180.2,


[PMID 478975] Hemoglobin Dunn: alpha 6 (A4) aspartic acid replaced by asparagine.


[PMID 3354560] Asymptomatic association of hemoglobin Dunn (alpha 6[A4]Asp----Asn) and hemoglobin O-Arab (beta 121[GH4]Glu----Lys) in a Moroccan man.


[PMID 6668192] Two rare alpha chain variants, Hb Dunn or alpha 26(A4)Asp replaced by Asn beta 2 and Hb G-Pest or alpha 274(EF3)Asp replaced by Asn beta 2, observed in an Indian and a black newborn.


[PMID 7435503] Oxygen affinity and stability of hemoglobin Dunn alpha 6(A4)Asp replaced by Asn): use of isoelectric focusing in recognition of a new abnormal hemoglobin.


[PMID 3754246] Hemoglobin Woodville: alpha (2)6(A4) aspartic acid----tyrosine.