List of variants reported as likely pathogenic for malignant endocrine neoplasm by Human Genome Sequencing Center Clinical Lab, Baylor College of Medicine

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.1998G>T (p.Lys666Asn)	rs146646971	0.00003
NM_003000.3(SDHB):c.221A>C (p.Asp74Ala)	rs876658713	0.00001
NM_004168.4(SDHA):c.688del (p.Glu230fs)	rs1553998199
NM_004168.4(SDHA):c.944dup (p.Gly316fs)	rs1579402180
NM_020975.6(RET):c.3222dup (p.Val1075fs)	rs1838374810

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