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: rs10077823
rs10077823
LOC101929710 ; LOC107986362
2 5 96510626 intron variant A/G snv 0.43 0.700 1.000 1 2012 2012
dbSNP: rs10173167
rs10173167 		2 2 646767 intergenic variant G/A snv 0.82 0.700 1.000 1 2009 2009
dbSNP: rs10188334
rs10188334 		2 2 653874 regulatory region variant C/A;T snv 0.15 0.700 1.000 1 2009 2009
dbSNP: rs10193244
rs10193244 		2 2 647580 intergenic variant T/C snv 0.77 0.700 1.000 1 2009 2009
dbSNP: rs1026534
rs1026534
LOC101929710 ; LOC107986362
2 5 96519387 intron variant G/C snv 0.60 0.700 1.000 1 2012 2012
dbSNP: rs10476682
rs10476682
LOC101929710
2 5 96522554 intron variant A/G snv 0.38 0.700 1.000 1 2012 2012
dbSNP: rs11231111
rs11231111
AHNAK
2 11 62492533 intron variant C/T snv 0.15 0.700 1.000 1 2010 2010
dbSNP: rs113313252
rs113313252
TNNI3K ; FPGT-TNNI3K ; LRRC53
2 1 74534327 intron variant -/T delins 0.700 1.000 1 2013 2013
dbSNP: rs1211166
rs1211166
NTRK2
2 9 84671077 intron variant G/A snv 0.77 0.700 1.000 1 2013 2013
dbSNP: rs12142020
rs12142020
TNNI3K ; FPGT-TNNI3K ; LRRC53
2 1 74534327 intron variant A/T snv 0.50 0.700 1.000 1 2013 2013
dbSNP: rs12525532
rs12525532
ANKS1A
2 6 35037042 intron variant C/T snv 0.33 0.700 1.000 1 2012 2012
dbSNP: rs12617233
rs12617233
LINC01122
2 2 58812863 intron variant T/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs12714414
rs12714414 		2 2 651407 intergenic variant T/C snv 0.18 0.700 1.000 1 2009 2009
dbSNP: rs12999687
rs12999687
DNMT3A
2 2 25289569 intron variant T/G snv 0.48 0.700 1.000 1 2012 2012
dbSNP: rs13034723
rs13034723
C2orf88
2 2 190120954 intron variant G/A snv 0.37 0.700 1.000 1 2012 2012
dbSNP: rs1320336
rs1320336 		2 2 650012 intergenic variant G/A snv 0.18 0.700 1.000 1 2009 2009
dbSNP: rs1320337
rs1320337 		2 2 649867 intergenic variant A/T snv 0.19 0.700 1.000 1 2009 2009
dbSNP: rs1320338
rs1320338 		2 2 649347 intergenic variant T/G snv 0.18 0.700 1.000 1 2009 2009
dbSNP: rs13386517
rs13386517 		2 2 650479 regulatory region variant G/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs13386627
rs13386627 		2 2 650560 regulatory region variant G/C;T snv 0.700 1.000 1 2009 2009
dbSNP: rs13386964
rs13386964 		2 2 650828 regulatory region variant G/A snv 0.18 0.700 1.000 1 2009 2009
dbSNP: rs13388043
rs13388043 		2 2 637597 regulatory region variant C/A;T snv 0.700 1.000 1 2009 2009
dbSNP: rs13393304
rs13393304 		2 2 637830 regulatory region variant A/C;G snv 0.700 1.000 1 2009 2009
dbSNP: rs13397165
rs13397165 		2 2 653354 intergenic variant G/A snv 0.18 0.700 1.000 1 2009 2009
dbSNP: rs13401686
rs13401686 		2 2 650519 regulatory region variant A/G snv 0.18 0.700 1.000 1 2009 2009