List of variants reported as likely benign for Peutz-Jeghers syndrome; Melanoma, cutaneous malignant, susceptibility to, 1; Familial pancreatic carcinoma; Germ cell tumor of testis

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_000455.5(STK11):c.894C>A (p.Phe298Leu)	rs199681533	0.00092
NM_000455.5(STK11):c.357C>T (p.Asn119=)	rs372511774	0.00007
NM_000455.5(STK11):c.42G>A (p.Glu14=)	rs758769888	0.00004
NM_000455.5(STK11):c.612C>T (p.Phe204=)	rs774100153	0.00004
NM_000455.5(STK11):c.651G>A (p.Pro217=)	rs368348370	0.00003
NM_000455.5(STK11):c.726G>A (p.Gly242=)	rs776823114	0.00001
NM_000455.5(STK11):c.846C>G (p.Leu282=)	rs777872290	0.00001
NM_000455.5(STK11):c.615G>T (p.Ala205=)
NM_000455.5(STK11):c.726G>T (p.Gly242=)	rs776823114

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