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rs35431217

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs35431217(A;C)
Make rs35431217(C;C)
ReferenceGRCh38 38.1/141
Chromosome16
Position173554
GeneHBA2
is asnp
is mentioned by
dbSNPrs35431217
ebirs35431217
HLIrs35431217
Exacrs35431217
Varsomers35431217
Maprs35431217
PheGenIrs35431217
hapmaprs35431217
1000 genomesrs35431217
hgdprs35431217
ensemblrs35431217
gopubmedrs35431217
geneviewrs35431217
scholarrs35431217
googlers35431217
pharmgkbrs35431217
gwascentralrs35431217
openSNPrs35431217
23andMers35431217
23andMe allrs35431217
SNP Nexus

SNPshotrs35431217
SNPdbers35431217
MSV3drs35431217
GWAS Ctlgrs35431217
Max Magnitude0
OMIM141800
Desc
Variant0137
Relatedalso
ClinVar
Risk rs35431217(C;C)
Alt rs35431217(C;C)
Reference rs35431217(A;A)
Significance Untested
Disease
Variation info
Gene HBA2
CLNDBN
Reversed 0
HGVS NC_000016.9:g.223553A>C
CLNSRC
CLNACC



[PMID 4429670] Hemoglobin St. Claude or alpha2-127(H10)Lys leads to Thr-beta2.