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rs147499872(A;G)

From SNPedia
Variant of uncertain significance (ClinVar)
Is agenotype
ofrs147499872
GeneDNAH5
Chromosome5
Position13,916,424
mentionedby
Magnitude1
Geno Mag Summary
(A;A) 0 common in clinvar
(A;G) 1 Variant of uncertain significance (ClinVar)