List of variants reported as likely pathogenic for benign neoplasm by deCODE genetics, Amgen

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_017849.4(TMEM127):c.185C>A (p.Ser62Ter)
NM_017849.4(TMEM127):c.230del (p.Pro77fs)
NM_017849.4(TMEM127):c.2T>C (p.Met1Thr)
NM_017849.4(TMEM127):c.409+1G>T	rs121908825

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