List of variants reported as uncertain significance for Primary erythromelalgia; Neuropathy, hereditary sensory and autonomic, type 2A; Paroxysmal extreme pain disorder; Severe myoclonic epilepsy in infancy; Channelopathy-associated congenital insensitivity to pain, autosomal recessive; Generalized epilepsy with febrile seizures plus, type 7 by Fulgent Genetics, Fulgent Genetics

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Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_001365536.1(SCN9A):c.684C>G (p.Ile228Met)	rs71428908	0.00081
NM_001365536.1(SCN9A):c.4820C>T (p.Thr1607Ile)	rs200470541	0.00012
NM_001365536.1(SCN9A):c.3538A>G (p.Asn1180Asp)	rs750269576	0.00007
NM_001365536.1(SCN9A):c.1280T>C (p.Leu427Ser)	rs192406412	0.00006
NM_001365536.1(SCN9A):c.2006G>A (p.Arg669His)	rs200374987	0.00006
NM_001365536.1(SCN9A):c.184A>G (p.Ile62Val)	rs121908920	0.00004
NM_001365536.1(SCN9A):c.2351C>G (p.Thr784Ser)	rs200624920	0.00004
NM_001365536.1(SCN9A):c.1604C>T (p.Ser535Leu)	rs201354321	0.00003
NM_001365536.1(SCN9A):c.1238T>C (p.Ile413Thr)	rs200689195	0.00002
NM_001365536.1(SCN9A):c.553C>T (p.Arg185Cys)	rs202083986	0.00002
NM_001365536.1(SCN9A):c.5948G>T (p.Ser1983Ile)	rs770802841	0.00001
NM_001365536.1(SCN9A):c.4368C>G (p.Ile1456Met)	rs1362318488
NM_001365536.1(SCN9A):c.5820C>G (p.Asn1940Lys)	rs371454107

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