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rs34049890

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs34049890(C;C)
Make rs34049890(C;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position5249466
GeneHBG2, LOC100288908
is asnp
is mentioned by
dbSNPrs34049890
ebirs34049890
HLIrs34049890
Exacrs34049890
Varsomers34049890
Maprs34049890
PheGenIrs34049890
hapmaprs34049890
1000 genomesrs34049890
hgdprs34049890
ensemblrs34049890
gopubmedrs34049890
geneviewrs34049890
scholarrs34049890
googlers34049890
pharmgkbrs34049890
gwascentralrs34049890
openSNPrs34049890
23andMers34049890
23andMe allrs34049890
SNP Nexus

SNPshotrs34049890
SNPdbers34049890
MSV3drs34049890
GWAS Ctlgrs34049890
Max Magnitude0
OMIM142200
Desc
Variant0011
Relatedalso
OMIM142250
Desc
Variant0018
Relatedalso


ClinVar
Risk rs34049890(C;C)
Alt rs34049890(C;C)
Reference rs34049890(G;G)
Significance Other
Disease HEMOGLOBIN F (IWATA)
Variation info
Gene HBG1
CLNDBN HEMOGLOBIN F (IWATA)
Reversed 1
HGVS NC_000011.9:g.5270696C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000016155.1,



[PMID 6163752] Survey of cord blood hemoglobin in Japan and identification of two new gamma chain variants.