List of variants reported as uncertain significance for Frontotemporal dementia and/or amyotrophic lateral sclerosis 6

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Total variants: 30

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HGVS	dbSNP	gnomAD frequency
NM_007126.5(VCP):c.*1040T>C	rs188935092	0.00171
NM_007126.5(VCP):c.1584C>T (p.Ala528=)	rs147623367	0.00064
NM_007126.5(VCP):c.*4G>T	rs201091341	0.00052
NM_007126.5(VCP):c.*367G>A	rs768675930	0.00043
NM_007126.5(VCP):c.*700C>A	rs537730311	0.00035
NM_007126.5(VCP):c.-250C>T	rs886063894	0.00023
NM_007126.5(VCP):c.*347C>T	rs886063888	0.00013
NM_007126.5(VCP):c.*382C>T	rs749381324	0.00011
NM_007126.5(VCP):c.-215A>G	rs886063893	0.00011
NM_007126.5(VCP):c.*172C>G	rs886063890	0.00006
NM_007126.5(VCP):c.*217G>T	rs981870646	0.00006
NM_007126.5(VCP):c.*64C>T	rs553370942	0.00006
NM_007126.4(VCP):c.-370G>A	rs886063895	0.00005
NM_007126.5(VCP):c.*63G>A	rs969638105	0.00005
NM_007126.5(VCP):c.1360-6T>C	rs370296303	0.00004
NM_007126.5(VCP):c.384T>C (p.Gly128=)	rs367703031	0.00003
NM_007126.5(VCP):c.*184G>A	rs886063889	0.00001
NM_007126.5(VCP):c.*885G>A	rs925146670	0.00001
NM_007126.5(VCP):c.335A>G (p.Lys112Arg)	rs766787045	0.00001
NM_007126.5(VCP):c.446-4G>A	rs370700002	0.00001
NM_007126.5(VCP):c.697A>G (p.Ile233Val)	rs750335399	0.00001
NM_007126.5(VCP):c.*216G>A	rs567542622
NM_007126.5(VCP):c.*788G>A	rs886063887
NM_007126.5(VCP):c.-53C>T	rs369830702
NM_007126.5(VCP):c.1293C>T (p.Asp431=)	rs1828712869
NM_007126.5(VCP):c.130-9T>C	rs1828868223
NM_007126.5(VCP):c.1374G>C (p.Gln458His)	rs1060499674
NM_007126.5(VCP):c.185A>G (p.Lys62Arg)	rs886063892
NM_007126.5(VCP):c.591C>G (p.Ser197=)	rs866003333
NM_007126.5(VCP):c.794T>C (p.Phe265Ser)	rs1828756507

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