Have questions? Visit https://www.reddit.com/r/SNPedia

rs34259907

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs34259907(A;G)
Make rs34259907(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position177014
GeneHBA1
is asnp
is mentioned by
dbSNPrs34259907
ebirs34259907
HLIrs34259907
Exacrs34259907
Varsomers34259907
Maprs34259907
PheGenIrs34259907
hapmaprs34259907
1000 genomesrs34259907
hgdprs34259907
ensemblrs34259907
gopubmedrs34259907
geneviewrs34259907
scholarrs34259907
googlers34259907
pharmgkbrs34259907
gwascentralrs34259907
openSNPrs34259907
23andMers34259907
23andMe allrs34259907
SNP Nexus

SNPshotrs34259907
SNPdbers34259907
MSV3drs34259907
GWAS Ctlgrs34259907
Max Magnitude0
OMIM141800
Desc
Variant0024
Relatedalso
ClinVar
Risk rs34259907(G;G)
Alt rs34259907(G;G)
Reference rs34259907(A;A)
Significance Other
Disease HEMOGLOBIN DAGESTAN
Variation info
Gene HBA1
CLNDBN HEMOGLOBIN DAGESTAN
Reversed 0
HGVS NC_000016.9:g.227013A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000017011.2,


[PMID 6783600] A new hemoglobin variant: Hb Dagestan alpha 60(E9) Lys leads to Glu.