List of variants reported as likely benign for hereditary dementia by Counsyl

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Total variants: 32

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HGVS	dbSNP	gnomAD frequency
NM_000520.5(HEXA):c.-167G>A	rs77707876	0.01456
NM_000520.5(HEXA):c.-59G>A	rs147174351	0.00489
NM_000520.6(HEXA):c.673-13T>C	rs75211071	0.00438
NM_000520.6(HEXA):c.253+5074C>T	rs149661366	0.00322
NM_000520.6(HEXA):c.346+13C>T	rs200871198	0.00173
NM_000520.6(HEXA):c.1146+8G>A	rs201453018	0.00167
NM_000520.6(HEXA):c.1527-6T>C	rs199914308	0.00087
NM_000520.6(HEXA):c.-4G>A	rs766510036	0.00050
NM_000520.6(HEXA):c.1074-100T>C	rs868411141	0.00038
NM_000520.6(HEXA):c.1435G>A (p.Ala479Thr)	rs145012038	0.00038
NM_000520.6(HEXA):c.8G>C (p.Ser3Thr)	rs374524755	0.00031
NM_000520.6(HEXA):c.1073+41C>T	rs367719010	0.00027
NM_000520.6(HEXA):c.1421+14G>C	rs201497629	0.00019
NM_000521.4(HEXB):c.1614-14C>A	rs201448394	0.00019
NM_000520.6(HEXA):c.1073+51G>A	rs545676277	0.00016
NM_000520.6(HEXA):c.253+5107G>A	rs748336538	0.00013
NM_000520.6(HEXA):c.548T>A (p.Leu183His)	rs185797496	0.00011
NM_000520.6(HEXA):c.1397A>G (p.Asn466Ser)	rs200936836	0.00009
NM_000391.4(TPP1):c.1125C>T (p.Arg375=)	rs587780972	0.00005
NM_000520.6(HEXA):c.1074-86G>A	rs1050913691	0.00001
NM_000520.6(HEXA):c.1421+13G>A	rs375201437	0.00001
NM_000784.4(CYP27A1):c.882G>A (p.Glu294=)	rs59428328	0.00001
NM_000391.4(TPP1):c.1267-56_1267-37del	rs1554901606
NM_000520.6(HEXA):c.1421+11del	rs922064515
NM_000520.6(HEXA):c.1421+13dup	rs780193130
NM_000520.6(HEXA):c.1421+15G>C	rs185764548
NM_000520.6(HEXA):c.1421+15G>T	rs185764548
NM_001042432.2(CLN3):c.582G>T (p.Leu194=)	rs386833734
NM_001042432.2(CLN3):c.963-63_963-44dup	rs1555468153
NM_018941.4(CLN8):c.507C>T (p.Ser169=)	rs386834131
NM_033305.3(VPS13A):c.9189+2545TGA[6]	rs113052866
NM_033305.3(VPS13A):c.9189+2545TGA[9]	rs113052866

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