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rs34890875

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs34890875(A;T)
Make rs34890875(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position176957
GeneHBA1
is asnp
is mentioned by
dbSNPrs34890875
ebirs34890875
HLIrs34890875
Exacrs34890875
Varsomers34890875
Maprs34890875
PheGenIrs34890875
hapmaprs34890875
1000 genomesrs34890875
hgdprs34890875
ensemblrs34890875
gopubmedrs34890875
geneviewrs34890875
scholarrs34890875
googlers34890875
pharmgkbrs34890875
gwascentralrs34890875
openSNPrs34890875
23andMers34890875
23andMe allrs34890875
SNP Nexus

SNPshotrs34890875
SNPdbers34890875
MSV3drs34890875
GWAS Ctlgrs34890875
Max Magnitude0
OMIM141800
Desc
Variant0099
Relatedalso
ClinVar
Risk rs34890875(T;T)
Alt rs34890875(T;T)
Reference rs34890875(A;A)
Significance Other
Disease HEMOGLOBIN MIYANO
Variation info
Gene HBA1
CLNDBN HEMOGLOBIN MIYANO
Reversed 0
HGVS NC_000016.9:g.226956A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017115.2,



[PMID 2634665] Hb Miyano or alpha 41(C6)Thr----Ser: a new high oxygen affinity alpha chain variant found in an erythremic blood donor.