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rs34879587

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs34879587(A;A)
Make rs34879587(A;C)
ReferenceGRCh38 38.1/141
Chromosome16
Position177081
GeneHBA1
is asnp
is mentioned by
dbSNPrs34879587
ebirs34879587
HLIrs34879587
Exacrs34879587
Varsomers34879587
Maprs34879587
PheGenIrs34879587
hapmaprs34879587
1000 genomesrs34879587
hgdprs34879587
ensemblrs34879587
gopubmedrs34879587
geneviewrs34879587
scholarrs34879587
googlers34879587
pharmgkbrs34879587
gwascentralrs34879587
openSNPrs34879587
23andMers34879587
23andMe allrs34879587
SNP Nexus

SNPshotrs34879587
SNPdbers34879587
MSV3drs34879587
GWAS Ctlgrs34879587
Max Magnitude0
OMIM141800
Desc
Variant0044
Relatedalso
ClinVar
Risk rs34879587(A;A)
Alt rs34879587(A;A)
Reference rs34879587(C;C)
Significance Other
Disease HEMOGLOBIN GARDEN STATE
Variation info
Gene HBA1
CLNDBN HEMOGLOBIN GARDEN STATE
Reversed 0
HGVS NC_000016.9:g.227080C>A
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000017036.2,