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: rs2075650
rs2075650
45 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.900 1.000 33 2009 2020
dbSNP: rs11136000
rs11136000
CLU
19 0.752 0.160 8 27607002 intron variant T/C snv 0.56 0.900 0.913 23 2009 2018
dbSNP: rs6656401
rs6656401
CR1
8 0.776 0.200 1 207518704 intron variant A/G;T snv 0.900 1.000 17 2009 2019
dbSNP: rs157580
rs157580
14 0.882 0.160 19 44892009 intron variant G/A snv 0.69 0.810 1.000 14 2009 2019
dbSNP: rs17070145
rs17070145
10 0.790 0.120 5 168418786 intron variant C/T snv 0.43 0.100 0.917 12 2009 2018
dbSNP: rs2373115
rs2373115
2 0.925 0.080 11 78380104 intron variant C/A snv 0.24 0.900 0.750 12 2007 2018
dbSNP: rs3764650
rs3764650
9 0.790 0.200 19 1046521 intron variant T/G snv 0.14 0.900 1.000 11 2011 2019
dbSNP: rs3818361
rs3818361
CR1
6 0.851 0.080 1 207611623 intron variant A/G snv 0.74 0.880 1.000 11 2009 2017
dbSNP: rs10524523
rs10524523
7 0.807 0.200 19 44899792 intron variant TTTTTTTTTTTTTTTTTTTTTTT/-;T;TT;TTT;TTTT;TTTTT;TTTTTT;TTTTTTT;TTTTTTTT;TTTTTTTTT;TTTTTTTTTT;TTTTTTTTTTT;TTTTTTTTTTTT;TTTTTTTTTTTTT;TTTTTTTTTTTTTT;TTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT delins 0.100 0.900 10 2012 2017
dbSNP: rs4147929
rs4147929
3 0.882 0.120 19 1063444 intron variant A/C;G snv 0.860 1.000 10 2013 2019
dbSNP: rs8106922
rs8106922
5 1.000 0.080 19 44898409 intron variant A/G snv 0.36 0.800 1.000 10 2009 2019
dbSNP: rs11218343
rs11218343
2 0.925 0.080 11 121564878 intron variant T/A;C snv 0.830 1.000 8 2013 2019
dbSNP: rs157582
rs157582
8 0.851 0.160 19 44892962 intron variant C/T snv 0.24 0.29 0.810 1.000 7 2010 2019
dbSNP: rs28834970
rs28834970
3 0.882 0.120 8 27337604 intron variant T/C snv 0.32 0.830 1.000 7 2013 2019
dbSNP: rs10410544
rs10410544
6 0.827 0.120 19 38894892 intron variant T/C snv 0.68 0.67 0.060 0.833 6 2013 2019
dbSNP: rs11771145
rs11771145
2 0.925 0.080 7 143413669 intron variant G/A snv 0.42 0.810 1.000 6 2011 2019
dbSNP: rs242557
rs242557
12 0.752 0.200 17 45942346 intron variant G/A snv 0.36 0.060 0.833 6 2008 2017
dbSNP: rs9331896
rs9331896
4 0.851 0.080 8 27610169 intron variant C/G;T snv 0.820 1.000 6 2013 2019
dbSNP: rs1476679
rs1476679
2 0.925 0.080 7 100406823 intron variant C/A;T snv 4.0E-06; 0.74 0.830 1.000 5 2013 2019
dbSNP: rs440277
rs440277
2 1.000 0.080 19 44857967 intron variant G/A snv 0.30 0.800 1.000 5 2009 2019
dbSNP: rs10498633
rs10498633
2 0.925 0.080 14 92460608 intron variant G/T snv 0.19 0.800 1.000 4 2013 2019
dbSNP: rs17125944
rs17125944
3 0.882 0.160 14 52933911 intron variant T/C snv 8.6E-02 0.830 1.000 4 2013 2018
dbSNP: rs1871047
rs1871047
2 1.000 0.080 19 44848489 intron variant A/G snv 0.31 0.700 1.000 4 2009 2014
dbSNP: rs2234693
rs2234693
77 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.040 1.000 4 2008 2014
dbSNP: rs2718058
rs2718058
2 0.925 0.080 7 37801932 intron variant A/G;T snv 0.820 1.000 4 2013 2019