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rs373145711(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs373145711
GeneASXL1
Chromosome20
Position32,433,408
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 8 Bohring-Opitz syndrome

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