List of variants reported as benign for Neuropathy, hereditary sensory and autonomic, type 2A

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Total variants: 24

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HGVS	dbSNP	gnomAD frequency
NM_018979.4(WNK1):c.6828C>T (p.Tyr2276=)	rs4766334	0.98898
NM_018979.4(WNK1):c.4517G>C (p.Cys1506Ser)	rs7955371	0.98791
NM_018979.4(WNK1):c.258T>C (p.Cys86=)	rs3168640	0.97485
NM_018979.4(WNK1):c.3166A>C (p.Thr1056Pro)	rs956868	0.84133
NM_018979.4(WNK1):c.1287A>G (p.Ala429=)	rs10774466	0.71926
NM_018979.4(WNK1):c.1153+40C>G	rs2158502	0.70364
NM_018979.4(WNK1):c.2328G>A (p.Gln776=)	rs1012729	0.69706
NM_213655.5(WNK1):c.2268T>C (p.Pro756=)	rs7300829	0.63713
NM_018979.4(WNK1):c.759+27G>A	rs3858703	0.61933
NM_018979.4(WNK1):c.5509+83A>G	rs2255390	0.57410
NM_213655.5(WNK1):c.2220dup (p.Phe741fs)	rs11441897	0.55139
NM_018979.4(WNK1):c.5424G>T (p.Met1808Ile)	rs12828016	0.40719
NM_018979.4(WNK1):c.3960C>T (p.Asn1320=)	rs7300444	0.39881
NM_018979.4(WNK1):c.5583+36C>T	rs2301880	0.24814
NM_018979.4(WNK1):c.1401-11C>A	rs11064573	0.12417
NM_018979.4(WNK1):c.1479T>C (p.Asp493=)	rs2286006	0.12413
NM_018979.4(WNK1):c.4044C>T (p.Thr1348=)	rs10849577	0.12407
NM_018979.4(WNK1):c.3489+4C>T	rs34032084	0.09932
NM_018979.4(WNK1):c.421G>A (p.Ala141Thr)	rs11554421	0.09867
NM_018979.4(WNK1):c.1994C>T (p.Thr665Ile)	rs2286007	0.05498
NM_001365536.1(SCN9A):c.2248A>G (p.Ile750Val)	rs182650126	0.00270
NM_001365536.1(SCN9A):c.2392A>G (p.Met798Val)	rs149707354	0.00097
NM_001365536.1(SCN9A):c.1975-3dup	rs35888674
NM_018979.4(WNK1):c.2373+21dup	rs5795952

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