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rs33974602

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs33974602(A;A)
Make rs33974602(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position5249561
GeneHBG1
is asnp
is mentioned by
dbSNPrs33974602
ebirs33974602
HLIrs33974602
Exacrs33974602
Varsomers33974602
Maprs33974602
PheGenIrs33974602
hapmaprs33974602
1000 genomesrs33974602
hgdprs33974602
ensemblrs33974602
gopubmedrs33974602
geneviewrs33974602
scholarrs33974602
googlers33974602
pharmgkbrs33974602
gwascentralrs33974602
openSNPrs33974602
23andMers33974602
23andMe allrs33974602
SNP Nexus

SNPshotrs33974602
SNPdbers33974602
MSV3drs33974602
GWAS Ctlgrs33974602
Max Magnitude0
OMIM142200
Desc
Variant0033
Relatedalso
OMIM142250
Desc
Variant0030
Relatedalso
ClinVar
Risk rs33974602(A;A)
Alt rs33974602(A;A)
Reference rs33974602(G;G)
Significance Other
Disease HEMOGLOBIN F (WOODSTOCK)
Variation info
Gene HBG1
CLNDBN HEMOGLOBIN F (WOODSTOCK)
Reversed 1
HGVS NC_000011.9:g.5270791C>T
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000016181.1,



[PMID 1802881] Gamma chain abnormalities and gamma-globin gene rearrangements in newborn babies of various populations.