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rs34127117

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs34127117(A;G)
Make rs34127117(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position5249390
GeneHBG1
is asnp
is mentioned by
dbSNPrs34127117
ebirs34127117
HLIrs34127117
Exacrs34127117
Varsomers34127117
Maprs34127117
PheGenIrs34127117
hapmaprs34127117
1000 genomesrs34127117
hgdprs34127117
ensemblrs34127117
gopubmedrs34127117
geneviewrs34127117
scholarrs34127117
googlers34127117
pharmgkbrs34127117
gwascentralrs34127117
openSNPrs34127117
23andMers34127117
23andMe allrs34127117
SNP Nexus

SNPshotrs34127117
SNPdbers34127117
MSV3drs34127117
GWAS Ctlgrs34127117
Max Magnitude0
OMIM142200
Desc
Variant0008
Relatedalso
ClinVar
Risk rs34127117(G;G)
Alt rs34127117(G;G)
Reference rs34127117(A;A)
Significance Other
Disease HEMOGLOBIN F (DICKINSON)
Variation info
Gene HBG1
CLNDBN HEMOGLOBIN F (DICKINSON)
Reversed 1
HGVS NC_000011.9:g.5270620T>C
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000016152.1,