List of variants in gene SCN9A studied for neuropathy, small fiber

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_001365536.1(SCN9A):c.444A>G (p.Pro148=)	rs9646771	0.69145
NM_001365536.1(SCN9A):c.174G>A (p.Gln58=)	rs6432901	0.63691
NM_001365536.1(SCN9A):c.688+13T>C	rs74449889	0.04864
NM_001365536.1(SCN9A):c.-294T>C	rs141521157	0.00704
NM_001365536.1(SCN9A):c.554G>A (p.Arg185His)	rs73969684	0.00574
NM_001365536.1(SCN9A):c.-126G>C	rs200099565	0.00068
NM_001365536.1(SCN9A):c.129T>C (p.Asp43=)	rs200826539	0.00019
NM_001365536.1(SCN9A):c.213G>A (p.Val71=)	rs200240989	0.00008
NM_001365536.1(SCN9A):c.685C>A (p.Pro229Thr)	rs755653914	0.00001
NM_002977.3(SCN9A):c.-339G>C	rs886055057	0.00001
NM_001365536.1(SCN9A):c.-290T>C	rs148362057
NM_001365536.1(SCN9A):c.274A>T (p.Asn92Tyr)	rs747265095
NM_002977.3(SCN9A):c.-324C>T	rs201905758

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