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rs34915311

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs34915311(G;G)
Make rs34915311(G;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position5254440
GeneHBG2, LOC100288908
is asnp
is mentioned by
dbSNPrs34915311
ebirs34915311
HLIrs34915311
Exacrs34915311
Varsomers34915311
Maprs34915311
PheGenIrs34915311
hapmaprs34915311
1000 genomesrs34915311
hgdprs34915311
ensemblrs34915311
gopubmedrs34915311
geneviewrs34915311
scholarrs34915311
googlers34915311
pharmgkbrs34915311
gwascentralrs34915311
openSNPrs34915311
23andMers34915311
23andMe allrs34915311
SNP Nexus

SNPshotrs34915311
SNPdbers34915311
MSV3drs34915311
GWAS Ctlgrs34915311
Max Magnitude0
OMIM142250
Desc
Variant0010
Relatedalso
ClinVar
Risk rs34915311(G;G)
Alt rs34915311(G;G)
Reference rs34915311(T;T)
Significance Other
Disease HEMOGLOBIN F (KINGSTON)
Variation info
Gene HBG2
CLNDBN HEMOGLOBIN F (KINGSTON)
Reversed 1
HGVS NC_000011.9:g.5275670A>C
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000016106.1,



[PMID 2448270] Hb F-Kingston or alpha 2G gamma 2(55)(D6)Met----Arg in a Spanish newborn.


[PMID 6186522] Hb F Kingston (G gamma 55 [D6] Met leads to Arg).