List of variants reported as uncertain significance for Neuropathy, hereditary sensory and autonomic, type 2A by Centre for Mendelian Genomics, University Medical Centre Ljubljana

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Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_001365536.1(SCN9A):c.684C>G (p.Ile228Met)	rs71428908	0.00078
NM_001365536.1(SCN9A):c.3349G>T (p.Val1117Leu)	rs200817435	0.00009
NM_001365536.1(SCN9A):c.2129G>A (p.Cys710Tyr)	rs201709980	0.00007
NM_001244008.2(KIF1A):c.5105G>A (p.Arg1702His)	rs369839651	0.00003
NM_001244008.2(KIF1A):c.3064-13C>T	rs779347174	0.00001
NM_001244008.2(KIF1A):c.3640+12C>T	rs1403885809	0.00001
NM_001244008.2(KIF1A):c.3670C>T (p.Arg1224Trp)	rs368577433	0.00001
NM_001244008.2(KIF1A):c.393C>A (p.Asn131Lys)	rs35139906
NM_001244008.2(KIF1A):c.4537C>G (p.Leu1513Val)	rs2045537723
NM_001244008.2(KIF1A):c.527C>T (p.Pro176Leu)	rs2054754659
NM_001365536.1(SCN9A):c.2299C>T (p.Pro767Ser)	rs199715588
NM_001365536.1(SCN9A):c.4243G>A (p.Ala1415Thr)	rs1694897566
NM_001365536.1(SCN9A):c.5588T>C (p.Met1863Thr)	rs201561928
NM_018979.4(WNK1):c.5572G>A (p.Gly1858Arg)	rs1395162926

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