Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs8106922
rs8106922
TOMM40
5 1.000 0.080 19 44898409 intron variant A/G snv 0.36 0.800 1.000 10 2009 2019
dbSNP: rs10402271
rs10402271 		7 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 0.800 1.000 9 2009 2019
dbSNP: rs6733839
rs6733839
LOC105373605
2 1.000 0.080 2 127135234 regulatory region variant C/T snv 0.39 0.820 1.000 8 2013 2019
dbSNP: rs10792832
rs10792832 		2 1.000 0.080 11 86156833 downstream gene variant A/G snv 0.70 0.800 1.000 6 2011 2019
dbSNP: rs3752246
rs3752246
ABCA7
2 1.000 0.080 19 1056493 missense variant G/C;T snv 0.84; 4.1E-06 0.850 0.833 6 2011 2019
dbSNP: rs143332484
rs143332484
TREM2 ; LOC105375056
1 1.000 0.080 6 41161469 missense variant C/A;T snv 7.6E-03 0.740 0.800 5 2015 2019
dbSNP: rs2234255
rs2234255
TREM2 ; TREML1 ; LOC105375056
1 1.000 0.080 6 41159805 missense variant G/A snv 4.9E-03 1.8E-03 0.050 1.000 5 2016 2019
dbSNP: rs440277
rs440277
NECTIN2
2 1.000 0.080 19 44857967 intron variant G/A snv 0.30 0.800 1.000 5 2009 2019
dbSNP: rs9271192
rs9271192 		1 1.000 0.080 6 32610753 intergenic variant C/A snv 0.74 0.810 1.000 5 2013 2019
dbSNP: rs1366541089
rs1366541089
CTSD
1 1.000 0.080 11 1754930 missense variant G/A snv 7.0E-06 0.040 0.500 4 2004 2015
dbSNP: rs1871047
rs1871047
NECTIN2
2 1.000 0.080 19 44848489 intron variant A/G snv 0.31 0.700 1.000 4 2009 2014
dbSNP: rs2282649
rs2282649
SORL1
1 1.000 0.080 11 121608249 non coding transcript exon variant C/T snv 0.27 0.040 1.000 4 2009 2019
dbSNP: rs2965101
rs2965101 		6 1.000 0.080 19 44734556 intergenic variant T/C snv 0.34 0.700 1.000 4 2009 2012
dbSNP: rs405697
rs405697
TOMM40
1 1.000 0.080 19 44901434 3 prime UTR variant A/G;T snv 0.800 1.000 4 2011 2019
dbSNP: rs7254776
rs7254776
LOC107985305
1 1.000 0.080 19 44724478 intron variant T/C;G snv 0.800 1.000 4 2009 2018
dbSNP: rs7920721
rs7920721
LOC105376412 ; LOC105376413
1 1.000 0.080 10 11678309 upstream gene variant A/G snv 0.31 0.810 1.000 4 2013 2019
dbSNP: rs8103315
rs8103315
BCL3
2 1.000 0.080 19 44750911 intron variant C/A snv 9.1E-02 0.800 1.000 4 2011 2018
dbSNP: rs9349407
rs9349407
CD2AP
2 1.000 0.080 6 47485642 intron variant G/C snv 0.23 0.830 1.000 4 2011 2015
dbSNP: rs10793294
rs10793294
GAB2
1 1.000 0.080 11 78285357 intron variant C/A;G snv 0.710 1.000 3 2007 2011
dbSNP: rs10948363
rs10948363
CD2AP
1 1.000 0.080 6 47520026 intron variant A/G snv 0.23 0.800 1.000 3 2013 2019
dbSNP: rs115550680
rs115550680
ABCA7
1 1.000 0.080 19 1050421 intron variant A/G snv 1.7E-02 0.830 0.667 3 2013 2019
dbSNP: rs11673139
rs11673139
NECTIN2
2 1.000 0.080 19 44879780 intron variant A/T snv 8.8E-02 0.700 1.000 3 2009 2012
dbSNP: rs12610605
rs12610605
NECTIN2
2 1.000 0.080 19 44867581 intron variant G/A snv 0.15 0.700 1.000 3 2010 2013
dbSNP: rs1303864231
rs1303864231
NANOG
1 1.000 0.080 12 7789754 missense variant A/G snv 4.0E-06 4.9E-05 0.030 1.000 3 2016 2018
dbSNP: rs17643262
rs17643262
MARK4 ; PPP1R37
1 1.000 0.080 19 45128558 intron variant G/A snv 9.9E-02 0.800 1.000 3 2011 2018