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: rs11730235
rs11730235
STIM2
1 4 26922822 intron variant G/T snv 0.26 0.700 1.000 1 2011 2011
dbSNP: rs6844153
rs6844153
STIM2
1 4 26942692 intron variant C/T snv 0.17 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: rs17606561
rs17606561
ELOVL2
2 1.000 0.040 6 10982126 3 prime UTR variant G/A snv 0.17 0.800 1.000 2 2011 2012
dbSNP: rs1007323
rs1007323
SYCP2L ; LOC101928191
1 6 10953011 intron variant T/A;G snv 0.700 1.000 1 2011 2011
dbSNP: rs10498676
rs10498676
ELOVL2
3 0.925 0.040 6 11026766 intron variant G/A snv 0.18 0.700 1.000 1 2011 2011
dbSNP: rs1061808
rs1061808
PPT2 ; AGPAT1 ; EGFL8 ; PPT2-EGFL8
2 6 32168770 3 prime UTR variant T/G snv 0.64 0.800 1.000 1 2012 2012
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: rs12526913
rs12526913 		1 6 11082691 downstream gene variant A/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs12529874
rs12529874 		2 6 98014625 intron variant G/A snv 2.6E-02 0.700 1.000 1 2013 2013
dbSNP: rs12662634
rs12662634
ELOVL2-AS1
1 6 11073958 intron variant G/A snv 0.17 0.700 1.000 1 2011 2011
dbSNP: rs12665478
rs12665478 		1 6 11080592 downstream gene variant G/A snv 0.41 0.700 1.000 1 2011 2011
dbSNP: rs1321535
rs1321535
ELOVL2-AS1
1 6 11075793 intron variant T/G snv 0.41 0.700 1.000 1 2011 2011