List of variants reported as pathogenic for cyanosis, transient neonatal

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_000184.2(HBG2):c.277C>T (p.His93Tyr)	rs35103459
NM_000184.3(HBG2):c.125T>C (p.Phe42Ser)	rs34878913
NM_000184.3(HBG2):c.190C>T (p.His64Tyr)	rs34474104
NM_000184.3(HBG2):c.191A>T (p.His64Leu)
NM_000184.3(HBG2):c.202G>A (p.Val68Met)	rs587776864
NM_000184.3(HBG2):c.85C>A (p.Leu29Met)	rs1278163109

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