ABO > ABO*O.01.25
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Phenotypes
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A,B
A1
Genetic Changes
nt change aa change Exon/Intron HGVS hg19 hg38 rsNum gnomAD
c.261delG p.Thr88Profs*31 Exon 6 chr9:136,132,909 chr9:133,257,493
 
c.454T>C Exon 7 chr9:136,131,664 chr9:133,256,248
 
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