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rs33931984

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs33931984(C;G)
Make rs33931984(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position176969
GeneHBA1
is asnp
is mentioned by
dbSNPrs33931984
ebirs33931984
HLIrs33931984
Exacrs33931984
Varsomers33931984
Maprs33931984
PheGenIrs33931984
hapmaprs33931984
1000 genomesrs33931984
hgdprs33931984
ensemblrs33931984
gopubmedrs33931984
geneviewrs33931984
scholarrs33931984
googlers33931984
pharmgkbrs33931984
gwascentralrs33931984
openSNPrs33931984
23andMers33931984
23andMe allrs33931984
SNP Nexus

SNPshotrs33931984
SNPdbers33931984
MSV3drs33931984
GWAS Ctlgrs33931984
Max Magnitude0
OMIM141800
Desc
Variant0176
Relatedalso
ClinVar
Risk rs33931984(G,T;G,T)
Alt rs33931984(G,T;G,T)
Reference rs33931984(C;C)
Significance Other
Disease HEMOGLOBIN POITIERS
Variation info
Gene HBA1
CLNDBN HEMOGLOBIN POITIERS
Reversed 0
HGVS NC_000016.9:g.226968C>G
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000017196.2,


[PMID 8195004] Hb Poitiers [alpha 45(CE3)His-->Asp]: a new hemoglobin variant with a two-fold increase in oxygen affinity.