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rs33917394

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs33917394(A;A)
Make rs33917394(A;C)
ReferenceGRCh38 38.1/142
Chromosome11
Position5225699
GeneHBB
is asnp
is mentioned by
dbSNPrs33917394
ebirs33917394
HLIrs33917394
Exacrs33917394
Varsomers33917394
Maprs33917394
PheGenIrs33917394
hapmaprs33917394
1000 genomesrs33917394
hgdprs33917394
ensemblrs33917394
gopubmedrs33917394
geneviewrs33917394
scholarrs33917394
googlers33917394
pharmgkbrs33917394
gwascentralrs33917394
openSNPrs33917394
23andMers33917394
23andMe allrs33917394
SNP Nexus

SNPshotrs33917394
SNPdbers33917394
MSV3drs33917394
GWAS Ctlgrs33917394
Max Magnitude0
OMIM141900
Desc
Variant0172
Relatedalso
OMIM141900
Desc
Variant0397
Relatedalso


ClinVar
Risk rs33917394(A;A)
Alt rs33917394(A;A)
Reference rs33917394(C;C)
Significance Other
Disease HEMOGLOBIN MASUDA HEMOGLOBIN ZENGCHENG
Variation info
Gene HBB
CLNDBN HEMOGLOBIN MASUDA HEMOGLOBIN ZENGCHENG
Reversed 1
HGVS NC_000011.9:g.5246929G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000016486.2, RCV000016745.2,



[PMID 2079435] Hb Zengcheng or alpha 2 beta(2)114(G16)Leu----Met.