Have questions? Visit https://www.reddit.com/r/SNPedia

rs33926206

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs33926206(A;C)
Make rs33926206(C;C)
ReferenceGRCh38 38.1/141
Chromosome16
Position177086
GeneHBA1
is asnp
is mentioned by
dbSNPrs33926206
ebirs33926206
HLIrs33926206
Exacrs33926206
Varsomers33926206
Maprs33926206
PheGenIrs33926206
hapmaprs33926206
1000 genomesrs33926206
hgdprs33926206
ensemblrs33926206
gopubmedrs33926206
geneviewrs33926206
scholarrs33926206
googlers33926206
pharmgkbrs33926206
gwascentralrs33926206
openSNPrs33926206
23andMers33926206
23andMe allrs33926206
SNP Nexus

SNPshotrs33926206
SNPdbers33926206
MSV3drs33926206
GWAS Ctlgrs33926206
Max Magnitude0
OMIM141800
Desc
Variant0030
Relatedalso
ClinVar
Risk rs33926206(C,G;C,G)
Alt rs33926206(C,G;C,G)
Reference rs33926206(A;A)
Significance Other
Disease HEMOGLOBIN ETOBICOKE
Variation info
Gene HBA1
CLNDBN HEMOGLOBIN ETOBICOKE
Reversed 0
HGVS NC_000016.9:g.227085A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000017017.2,


[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.