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rs33943087

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs33943087(A;G)
Make rs33943087(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position176778
GeneHBA1
is asnp
is mentioned by
dbSNPrs33943087
ebirs33943087
HLIrs33943087
Exacrs33943087
Varsomers33943087
Maprs33943087
PheGenIrs33943087
hapmaprs33943087
1000 genomesrs33943087
hgdprs33943087
ensemblrs33943087
gopubmedrs33943087
geneviewrs33943087
scholarrs33943087
googlers33943087
pharmgkbrs33943087
gwascentralrs33943087
openSNPrs33943087
23andMers33943087
23andMe allrs33943087
SNP Nexus

SNPshotrs33943087
SNPdbers33943087
MSV3drs33943087
GWAS Ctlgrs33943087
Max Magnitude0
OMIM141800
Desc
Variant0053
Relatedalso
ClinVar
Risk rs33943087(C,G;C,G)
Alt rs33943087(C,G;C,G)
Reference rs33943087(A;A)
Significance Other
Disease HEMOGLOBIN HOBART
Variation info
Gene HBA1
CLNDBN HEMOGLOBIN HOBART
Reversed 0
HGVS NC_000016.9:g.226777A>G
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000017049.2,


[PMID 3654264] Hemoglobin Hobart or alpha 20(Bl)His----Arg: a new alpha chain hemoglobin variant.


[PMID 11186259] Hb Anderlecht [alpha20(B1)His-->Pro]: a silent variant found in a Congolese newborn.