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rs34665886

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs34665886(C;G)
Make rs34665886(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position5226603
GeneHBB
is asnp
is mentioned by
dbSNPrs34665886
ebirs34665886
HLIrs34665886
Exacrs34665886
Varsomers34665886
Maprs34665886
PheGenIrs34665886
hapmaprs34665886
1000 genomesrs34665886
hgdprs34665886
ensemblrs34665886
gopubmedrs34665886
geneviewrs34665886
scholarrs34665886
googlers34665886
pharmgkbrs34665886
gwascentralrs34665886
openSNPrs34665886
23andMers34665886
23andMe allrs34665886
SNP Nexus

SNPshotrs34665886
SNPdbers34665886
MSV3drs34665886
GWAS Ctlgrs34665886
Max Magnitude0
OMIM141900
Desc
Variant0235
Relatedalso


ClinVar
Risk rs34665886(G;G)
Alt rs34665886(G;G)
Reference rs34665886(C;C)
Significance Other
Disease HEMOGLOBIN REGINA
Variation info
Gene HBB
CLNDBN HEMOGLOBIN REGINA
Reversed 1
HGVS NC_000011.9:g.5247833G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000016565.2,



[PMID 3839106] Hb Regina or alpha 2 beta 2 96(FG3)Leu----Val: a high oxygen affinity variant discovered by cation-exchange HPLC.