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: rs10488631
rs10488631
TNPO3
13 0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 0.800 1.000 5 2009 2015
dbSNP: rs1052587
rs1052587
MAPT
3 0.925 0.120 17 46025238 3 prime UTR variant T/C snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs1052590
rs1052590
MAPT
1 1.000 0.080 17 46025272 3 prime UTR variant A/G snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs1052594
rs1052594
MAPT
2 1.000 0.080 17 46025323 3 prime UTR variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs1054037
rs1054037
MANBA
1 1.000 0.080 4 102631552 3 prime UTR variant C/A;T snv 0.800 1.000 3 2011 2015
dbSNP: rs1054609
rs1054609
ZPBP2
2 0.925 0.160 17 39877024 3 prime UTR variant A/C snv 0.40 0.700 1.000 1 2012 2012
dbSNP: rs10607450
rs10607450 		1 1.000 0.080 11 118812058 regulatory region variant T/C snv 0.19 0.700 1.000 1 2012 2012
dbSNP: rs1076222
rs1076222
KANSL1
2 1.000 0.080 17 46032403 non coding transcript exon variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1077358
rs1077358
MANBA
1 1.000 0.080 4 102632769 intron variant C/T snv 0.55 0.700 1.000 1 2012 2012
dbSNP: rs1078268
rs1078268
MAPT ; STH
3 0.925 0.120 17 45998535 intron variant A/G snv 0.15 0.700 1.000 1 2012 2012
dbSNP: rs10843104
rs10843104
LOC105369710 ; LOC107984462
1 1.000 0.080 12 28123693 intergenic variant T/C snv 0.28 0.700 1.000 1 2012 2012
dbSNP: rs10852935
rs10852935
ZPBP2
1 1.000 0.080 17 39875421 synonymous variant C/T snv 0.40 0.35 0.700 1.000 1 2012 2012
dbSNP: rs10852936
rs10852936
ZPBP2
3 0.925 0.120 17 39875461 intron variant C/T snv 0.39 0.40 0.700 1.000 1 2012 2012
dbSNP: rs10889681
rs10889681
IL12RB2
2 0.925 0.160 1 67333487 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs10892294
rs10892294 		1 1.000 0.080 11 118796648 downstream gene variant G/C snv 0.19 0.700 1.000 1 2011 2011
dbSNP: rs10931468
rs10931468
NAB1
2 0.925 0.080 2 190673836 intron variant C/A;G;T snv 0.800 1.000 1 2011 2011
dbSNP: rs10982445
rs10982445
TNFSF8 ; DELEC1
1 1.000 0.080 9 114897411 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs11064157
rs11064157
LTBR
1 1.000 0.080 12 6383483 intron variant A/C snv 0.79 0.700 1.000 1 2012 2012
dbSNP: rs11065979
rs11065979 		12 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 0.800 1.000 1 2012 2012
dbSNP: rs11065987
rs11065987 		17 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 0.700 1.000 1 2015 2015
dbSNP: rs11078925
rs11078925
ZPBP2
3 0.925 0.160 17 39868955 intron variant T/C snv 0.36 0.700 1.000 1 2012 2012
dbSNP: rs11078928
rs11078928
GSDMB
2 0.925 0.160 17 39908216 splice acceptor variant T/A;C snv 0.40 0.700 1.000 1 2012 2012
dbSNP: rs11078929
rs11078929
PSMD3
1 1.000 0.080 17 39983981 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs11079725
rs11079725
SPPL2C ; MAPT-AS1
3 0.925 0.120 17 45846568 synonymous variant T/C snv 0.15 0.14 0.700 1.000 1 2012 2012
dbSNP: rs11079729
rs11079729
KANSL1
2 1.000 0.080 17 46038203 non coding transcript exon variant C/A;T snv 0.700 1.000 1 2012 2012