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rs35628685

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs35628685(A;A)
Make rs35628685(A;C)
ReferenceGRCh38 38.1/141
Chromosome16
Position176775
GeneHBA1
is asnp
is mentioned by
dbSNPrs35628685
ebirs35628685
HLIrs35628685
Exacrs35628685
Varsomers35628685
Maprs35628685
PheGenIrs35628685
hapmaprs35628685
1000 genomesrs35628685
hgdprs35628685
ensemblrs35628685
gopubmedrs35628685
geneviewrs35628685
scholarrs35628685
googlers35628685
pharmgkbrs35628685
gwascentralrs35628685
openSNPrs35628685
23andMers35628685
23andMe allrs35628685
SNP Nexus

SNPshotrs35628685
SNPdbers35628685
MSV3drs35628685
GWAS Ctlgrs35628685
Max Magnitude0
OMIM141800
Desc
Variant0076
Relatedalso
ClinVar
Risk rs35628685(A;A)
Alt rs35628685(A;A)
Reference rs35628685(C;C)
Significance Other
Disease HEMOGLOBIN J (TASHIKUERGAN)
Variation info
Gene HBA1
CLNDBN HEMOGLOBIN J (TASHIKUERGAN)
Reversed 0
HGVS NC_000016.9:g.226774C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017074.4,


[PMID 6548207] A new fast-moving hemoglobin variant, Hb J-Tashikuergan alpha 19(AB1) Ala----Glu.