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rs34868036

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs34868036(C;T)
Make rs34868036(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position177110
GeneHBA2
is asnp
is mentioned by
dbSNPrs34868036
ebirs34868036
HLIrs34868036
Exacrs34868036
Varsomers34868036
Maprs34868036
PheGenIrs34868036
hapmaprs34868036
1000 genomesrs34868036
hgdprs34868036
ensemblrs34868036
gopubmedrs34868036
geneviewrs34868036
scholarrs34868036
googlers34868036
pharmgkbrs34868036
gwascentralrs34868036
openSNPrs34868036
23andMers34868036
23andMe allrs34868036
SNP Nexus

SNPshotrs34868036
SNPdbers34868036
MSV3drs34868036
GWAS Ctlgrs34868036
Max Magnitude0
OMIM141800
Desc
Variant0185
Relatedalso
ClinVar
Risk rs34868036(T;T)
Alt rs34868036(T;T)
Reference rs34868036(C;C)
Significance Other
Disease HEMOGLOBIN CEMENELUM
Variation info
Gene HBA1
CLNDBN HEMOGLOBIN CEMENELUM
Reversed 0
HGVS NC_000016.9:g.227109C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017205.2,


[PMID 8148419] Hb Cemenelum [alpha 92 (FG4) Arg-->Trp]: a hemoglobin variant of the alpha 1/beta 2 interface that displays a moderate increase in oxygen affinity.