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: rs12936587
rs12936587 		5 0.882 0.080 17 17640408 regulatory region variant G/A snv 0.38 0.700 1.000 1 2013 2013
dbSNP: rs2047009
rs2047009 		2 0.925 0.080 10 44044465 regulatory region variant T/G snv 0.39 0.700 1.000 1 2013 2013
dbSNP: rs501120
rs501120 		10 0.763 0.240 10 44258419 downstream gene variant T/C snv 0.24 0.700 1.000 1 2013 2013
dbSNP: rs515135
rs515135 		9 0.807 0.160 2 21063185 intergenic variant T/C snv 0.73 0.700 1.000 1 2013 2013
dbSNP: rs579459
rs579459 		28 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 0.700 1.000 1 2013 2013
dbSNP: rs602633
rs602633 		10 0.851 0.080 1 109278889 downstream gene variant T/G snv 0.63 0.700 1.000 1 2013 2013
dbSNP: rs974819
rs974819 		6 0.807 0.080 11 103789839 intron variant T/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs9982601
rs9982601 		4 0.851 0.080 21 34226827 intron variant C/T snv 0.15 0.700 1.000 1 2013 2013
dbSNP: rs445925
rs445925
APOC1
10 0.882 0.080 19 44912383 non coding transcript exon variant G/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs1333049
rs1333049
CDKN2B-AS1
60 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.700 1.000 1 2013 2013
dbSNP: rs3217992
rs3217992
CDKN2B ; CDKN2B-AS1
22 0.683 0.480 9 22003224 3 prime UTR variant C/T snv 0.32 0.700 1.000 1 2013 2013
dbSNP: rs12413409
rs12413409
CNNM2
9 0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02 0.700 1.000 1 2013 2013
dbSNP: rs4773144
rs4773144
COL4A1 ; COL4A2
7 0.827 0.080 13 110308365 intron variant A/G snv 0.42 0.700 1.000 1 2013 2013
dbSNP: rs17514846
rs17514846
FURIN
7 0.882 0.120 15 90873320 intron variant C/A;G snv 0.700 1.000 1 2013 2013
dbSNP: rs2642
rs2642
GOT1
1 1.000 0.080 10 99396992 3 prime UTR variant T/C snv 5.0E-02 0.700 1.000 1 2013 2013
dbSNP: rs2895811
rs2895811
HHIPL1
4 0.851 0.080 14 99667605 intron variant T/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs4845625
rs4845625
IL6R
9 0.851 0.080 1 154449591 intron variant T/C snv 0.60 0.700 1.000 1 2013 2013
dbSNP: rs10947789
rs10947789
KCNK5
2 0.925 0.080 6 39207146 intron variant T/C snv 0.18 0.700 1.000 1 2013 2013
dbSNP: rs11203042
rs11203042
LIPA
1 1.000 0.080 10 89229352 intron variant T/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs2246833
rs2246833
LIPA
3 0.882 0.080 10 89246097 intron variant C/T snv 0.38 0.700 1.000 1 2013 2013
dbSNP: rs3798220
rs3798220
LPA
16 0.732 0.160 6 160540105 missense variant T/C snv 5.6E-02 3.1E-02 0.700 1.000 1 2013 2013
dbSNP: rs121918529
rs121918529
MEF2A
3 0.882 0.080 15 99690400 missense variant C/T snv 6.1E-04 6.5E-04 0.700 0
dbSNP: rs121918531
rs121918531
MEF2A
2 0.925 0.080 15 99690412 missense variant G/A snv 8.3E-06 2.1E-05 0.700 0
dbSNP: rs7173743
rs7173743
MORF4L1
6 0.851 0.120 15 78849442 intron variant T/C snv 0.45 0.700 1.000 1 2013 2013
dbSNP: rs9818870
rs9818870
MRAS
9 0.807 0.200 3 138403280 3 prime UTR variant C/A;T snv 0.700 1.000 1 2013 2013