List of variants reported as uncertain significance for Small fiber neuropathy

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Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 26

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HGVS	dbSNP	gnomAD frequency
NM_001365536.1(SCN9A):c.*1770A>C	rs200353065	0.00115
NM_001365536.1(SCN9A):c.-126G>C	rs200099565	0.00068
NM_001365536.1(SCN9A):c.1980G>A (p.Thr660=)	rs200014315	0.00023
NM_001365536.1(SCN9A):c.213G>A (p.Val71=)	rs200240989	0.00008
NM_001365536.1(SCN9A):c.4503+8_4503+9insT	rs767624579	0.00003
NM_001365536.1(SCN9A):c.685C>A (p.Pro229Thr)	rs755653914	0.00003
NM_001365536.1(SCN9A):c.*2744del	rs763459885	0.00002
NM_001365536.1(SCN9A):c.*948G>A	rs201415802	0.00002
NM_001365536.1(SCN9A):c.*2860C>T	rs200963393	0.00001
NM_001365536.1(SCN9A):c.1347T>C (p.Ser449=)	rs201990547	0.00001
NM_001365536.1(SCN9A):c.1713C>T (p.Ala571=)	rs200876333	0.00001
NM_001365536.1(SCN9A):c.3464T>A (p.Phe1155Tyr)	rs750839038	0.00001
NM_001365536.1(SCN9A):c.3497G>A (p.Cys1166Tyr)	rs370455223	0.00001
NM_001365536.1(SCN9A):c.165_167dup	rs886055049
NM_001365536.1(SCN9A):c.*226A>C	rs886055048
NM_001365536.1(SCN9A):c.*3282A>C	rs139483482
NM_001365536.1(SCN9A):c.*491del	rs886055047
NM_001365536.1(SCN9A):c.1014T>G (p.Asp338Glu)	rs886055056
NM_001365536.1(SCN9A):c.1094A>G (p.Asn365Ser)	rs886055055
NM_001365536.1(SCN9A):c.274A>T (p.Asn92Tyr)	rs747265095
NM_001365536.1(SCN9A):c.2916T>C (p.Ser972=)	rs886055054
NM_001365536.1(SCN9A):c.3265G>A (p.Val1089Met)	rs886055053
NM_001365536.1(SCN9A):c.3754A>G (p.Thr1252Ala)	rs886055052
NM_001365536.1(SCN9A):c.4434GAA[1] (p.Lys1480del)	rs886055050
NM_002977.3(SCN9A):c.-324C>T	rs201905758
NM_002977.3(SCN9A):c.-339G>C	rs886055057

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