List of variants reported as likely pathogenic for hereditary dementia by O&I group, Department of Genetics, University Medical Center of Groningen

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_004977.3(KCNC3):c.1771A>G (p.Ser591Gly)	rs549394447	0.00331
NM_006392.4(NOP56):c.909G>A (p.Ala303=)	rs1295942947	0.00001
NM_001127222.2(CACNA1A):c.2345G>C (p.Arg782Pro)	rs1233611505
NM_001127222.2(CACNA1A):c.4979G>A (p.Arg1660His)	rs121908216
NM_001378969.1(KCND3):c.1291C>T (p.Arg431Cys)	rs777183510
NM_002739.5(PRKCG):c.715C>T (p.Arg239Trp)	rs1471641294
NM_007289.4(MME):c.1095-2A>C	rs2108312675
NM_018896.5(CACNA1G):c.3792G>T (p.Arg1264Ser)	rs200024646
NM_173500.4(TTBK2):c.3466C>T (p.Arg1156Ter)	rs770444240

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