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: rs1007323
rs1007323
SYCP2L ; LOC101928191
1 6 10953011 intron variant T/A;G snv 0.700 1.000 1 2011 2011
dbSNP: rs10220265
rs10220265 		1 13 103397233 downstream gene variant G/A snv 0.28 0.700 1.000 1 2011 2011
dbSNP: rs10404486
rs10404486
ZNF600
1 19 52780882 non coding transcript exon variant C/T snv 0.20 0.800 1.000 1 2012 2012
dbSNP: rs1058694
rs1058694
AGPAT3
1 21 43984239 3 prime UTR variant C/T snv 0.32 0.700 1.000 1 2011 2011
dbSNP: rs10769780
rs10769780
SYT9
1 11 7345864 intron variant T/C snv 0.25 0.800 1.000 1 2012 2012
dbSNP: rs10792320
rs10792320 		1 11 61978819 intergenic variant A/C;T snv 0.700 1.000 1 2011 2011
dbSNP: rs10897208
rs10897208 		1 11 62024415 intergenic variant A/T snv 0.11 0.700 1.000 1 2011 2011
dbSNP: rs11230874
rs11230874 		1 11 62028114 intergenic variant T/G snv 6.9E-02 0.700 1.000 1 2011 2011
dbSNP: rs1145652
rs1145652 		1 5 165337081 intergenic variant A/G snv 9.6E-02 0.700 1.000 1 2011 2011
dbSNP: rs11662721
rs11662721
ABHD3
1 18 21681452 intron variant C/T snv 0.15 0.800 1.000 1 2012 2012
dbSNP: rs11730235
rs11730235
STIM2
1 4 26922822 intron variant G/T snv 0.26 0.700 1.000 1 2011 2011
dbSNP: rs12190237
rs12190237
SYCP2L
1 6 10922405 intron variant G/A snv 0.24 0.700 1.000 1 2011 2011
dbSNP: rs12195587
rs12195587
ELOVL2
1 6 10989709 synonymous variant G/A snv 0.12 0.11 0.700 1.000 1 2011 2011
dbSNP: rs12199131
rs12199131
SYCP2L ; LOC101928191
1 6 10932336 intron variant G/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs12200867
rs12200867
SYCP2L ; LOC101928191
1 6 10939591 intron variant C/G snv 0.22 0.700 1.000 1 2011 2011
dbSNP: rs12207488
rs12207488
SYCP2L ; LOC101928191
1 6 10952103 intron variant G/A snv 0.19 0.700 1.000 1 2011 2011
dbSNP: rs12213249
rs12213249
SYCP2L
1 6 10926709 intron variant C/T snv 0.19 0.700 1.000 1 2011 2011
dbSNP: rs12214825
rs12214825
SYCP2L ; LOC101928191
1 6 10933145 intron variant C/T snv 0.20 0.700 1.000 1 2011 2011
dbSNP: rs1225717
rs1225717
SYCP2L
1 6 10978007 intron variant A/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs1225736
rs1225736
SYCP2L ; LOC101928191
1 6 10939156 intron variant A/G snv 0.24 0.700 1.000 1 2011 2011
dbSNP: rs1225737
rs1225737
ELOVL2
1 6 10982419 3 prime UTR variant C/T snv 0.59 0.700 1.000 1 2011 2011
dbSNP: rs1225741
rs1225741
SYCP2L ; LOC101928191
1 6 10952010 intron variant G/A snv 0.39 0.700 1.000 1 2011 2011
dbSNP: rs1225744
rs1225744
SYCP2L ; LOC101928191
1 6 10954307 intron variant C/T snv 0.35 0.700 1.000 1 2011 2011
dbSNP: rs1225753
rs1225753
SYCP2L
1 6 10956456 intron variant G/A snv 0.43 0.700 1.000 1 2011 2011
dbSNP: rs12423247
rs12423247 		1 12 96464584 intron variant A/T snv 9.2E-02 0.800 1.000 1 2012 2012