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rs33996798

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs33996798(C;G)
Make rs33996798(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position177088
GeneHBA1
is asnp
is mentioned by
dbSNPrs33996798
ebirs33996798
HLIrs33996798
Exacrs33996798
Varsomers33996798
Maprs33996798
PheGenIrs33996798
hapmaprs33996798
1000 genomesrs33996798
hgdprs33996798
ensemblrs33996798
gopubmedrs33996798
geneviewrs33996798
scholarrs33996798
googlers33996798
pharmgkbrs33996798
gwascentralrs33996798
openSNPrs33996798
23andMers33996798
23andMe allrs33996798
SNP Nexus

SNPshotrs33996798
SNPdbers33996798
MSV3drs33996798
GWAS Ctlgrs33996798
Max Magnitude0
OMIM141800
Desc
Variant0030
Relatedalso
ClinVar
Risk rs33996798(A,G;A,G)
Alt rs33996798(A,G;A,G)
Reference rs33996798(C;C)
Significance Untested
Disease
Variation info
Gene HBA1
CLNDBN
Reversed 0
HGVS NC_000016.9:g.227087C>A; NC_000016.9:g.227087C>G
CLNSRC
CLNACC


[PMID 5774804] Hemoglobin Etobicoke: alpha-84(F5) serine replaced by arginine.


[PMID 6874377] Hb Etobicoke, alpha 85(F5) Ser leads to Arg found in a newborn of French-Indian-English descent.