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rs35166834

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs35166834(G;G)
Make rs35166834(G;T)
ReferenceGRCh38 38.1/142
Chromosome16
Position177380
GeneHBA1
is asnp
is mentioned by
dbSNPrs35166834
ebirs35166834
HLIrs35166834
Exacrs35166834
Varsomers35166834
Maprs35166834
PheGenIrs35166834
hapmaprs35166834
1000 genomesrs35166834
hgdprs35166834
ensemblrs35166834
gopubmedrs35166834
geneviewrs35166834
scholarrs35166834
googlers35166834
pharmgkbrs35166834
gwascentralrs35166834
openSNPrs35166834
23andMers35166834
23andMe allrs35166834
SNP Nexus

SNPshotrs35166834
SNPdbers35166834
MSV3drs35166834
GWAS Ctlgrs35166834
Max Magnitude0
OMIM141800
Desc
Variant0178
Relatedalso


ClinVar
Risk rs35166834(G;G)
Alt rs35166834(G;G)
Reference rs35166834(T;T)
Significance Other
Disease HEMOGLOBIN CAEN
Variation info
Gene HBA1
CLNDBN HEMOGLOBIN CAEN
Reversed 0
HGVS NC_000016.9:g.227379T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000017197.2,



[PMID 8493987] Unstable alpha-chain hemoglobin variants with factitious beta-thalassemia biosynthetic ratio: Hb Questembert (alpha 131[H14]Ser-->Pro) and Hb Caen (alpha 132[H15]Val-->Gly).