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rs34608326

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs34608326(A;A)
Make rs34608326(A;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position176784
GeneHBA1
is asnp
is mentioned by
dbSNPrs34608326
ebirs34608326
HLIrs34608326
Exacrs34608326
Varsomers34608326
Maprs34608326
PheGenIrs34608326
hapmaprs34608326
1000 genomesrs34608326
hgdprs34608326
ensemblrs34608326
gopubmedrs34608326
geneviewrs34608326
scholarrs34608326
googlers34608326
pharmgkbrs34608326
gwascentralrs34608326
openSNPrs34608326
23andMers34608326
23andMe allrs34608326
SNP Nexus

SNPshotrs34608326
SNPdbers34608326
MSV3drs34608326
GWAS Ctlgrs34608326
Max Magnitude0
OMIM141800
Desc
Variant0067
Relatedalso
ClinVar
Risk rs34608326(A;A)
Alt rs34608326(A;A)
Reference rs34608326(G;G)
Significance Other
Disease HEMOGLOBIN J (MEDELLIN)
Variation info
Gene HBA1
CLNDBN HEMOGLOBIN J (MEDELLIN)
Reversed 0
HGVS NC_000016.9:g.226783G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017066.2,