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rs34019507

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs34019507(G;T)
Make rs34019507(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position5254409
GeneHBG2
is asnp
is mentioned by
dbSNPrs34019507
ebirs34019507
HLIrs34019507
Exacrs34019507
Varsomers34019507
Maprs34019507
PheGenIrs34019507
hapmaprs34019507
1000 genomesrs34019507
hgdprs34019507
ensemblrs34019507
gopubmedrs34019507
geneviewrs34019507
scholarrs34019507
googlers34019507
pharmgkbrs34019507
gwascentralrs34019507
openSNPrs34019507
23andMers34019507
23andMe allrs34019507
SNP Nexus

SNPshotrs34019507
SNPdbers34019507
MSV3drs34019507
GWAS Ctlgrs34019507
Max Magnitude0
OMIM142250
Desc
Variant0005
Relatedalso
ClinVar
Risk rs34019507(C,T;C,T)
Alt rs34019507(C,T;C,T)
Reference rs34019507(G;G)
Significance Other
Disease HEMOGLOBIN F (CLARKE)
Variation info
Gene HBG2
CLNDBN HEMOGLOBIN F (CLARKE)
Reversed 1
HGVS NC_000011.9:g.5275639C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000016101.1,


[PMID 2442123] Hb F-Clarke or alpha 2G gamma 2(65)(E9)Lys----Asn.