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rs35329201

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs35329201(A;G)
Make rs35329201(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position177293
GeneHBA1
is asnp
is mentioned by
dbSNPrs35329201
ebirs35329201
HLIrs35329201
Exacrs35329201
Varsomers35329201
Maprs35329201
PheGenIrs35329201
hapmaprs35329201
1000 genomesrs35329201
hgdprs35329201
ensemblrs35329201
gopubmedrs35329201
geneviewrs35329201
scholarrs35329201
googlers35329201
pharmgkbrs35329201
gwascentralrs35329201
openSNPrs35329201
23andMers35329201
23andMe allrs35329201
SNP Nexus

SNPshotrs35329201
SNPdbers35329201
MSV3drs35329201
GWAS Ctlgrs35329201
Max Magnitude0
OMIM141800
Desc
Variant0022
Relatedalso


ClinVar
Risk rs35329201(G;G)
Alt rs35329201(G;G)
Reference rs35329201(A;A)
Significance Other
Disease HEMOGLOBIN CONTALDO
Variation info
Gene HBA1
CLNDBN HEMOGLOBIN CONTALDO
Reversed 0
HGVS NC_000016.9:g.227292A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000017009.2,



[PMID 6547932] The characterization of hemoglobin Manitoba or alpha (2)102(G9)Ser----Arg beta 2 and hemoglobin Contaldo or alpha (2)103(G10)His----Arg beta 2 by high performance liquid chromatography.