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: rs17018311
rs17018311
INTS7
2 1.000 0.040 1 211981666 intron variant T/C snv 2.7E-02 0.700 1.000 1 2012 2012
dbSNP: rs285480
rs285480
RXRG
1 1 165434666 intron variant G/A snv 0.72 0.800 1.000 1 2011 2011
dbSNP: rs10932966
rs10932966 		1 2 222667020 upstream gene variant C/A snv 0.79 0.700 1.000 1 2012 2012
dbSNP: rs12614577
rs12614577
SGPP2
1 2 222554810 intron variant G/C snv 0.69 0.700 1.000 1 2012 2012
dbSNP: rs10428174
rs10428174
FHIT
1 3 59828322 intron variant G/A snv 0.72 0.700 1.000 1 2012 2012
dbSNP: rs1079196
rs1079196
FHIT
1 3 59821052 intron variant G/A snv 0.22 0.700 1.000 1 2012 2012
dbSNP: rs13080594
rs13080594
GRM7
1 3 7361959 intron variant C/G;T snv 0.800 1.000 1 2011 2011
dbSNP: rs16852815
rs16852815 		1 3 142914477 intron variant T/C snv 0.12 0.700 1.000 1 2010 2010
dbSNP: rs9846232
rs9846232
LINC00620
1 3 13701633 intron variant G/T snv 5.1E-02 0.800 1.000 1 2011 2011
dbSNP: rs9684265
rs9684265
CLNK
1 4 10588037 intron variant G/A snv 0.97 0.700 1.000 1 2012 2012
dbSNP: rs10479334
rs10479334 		1 5 105618627 intergenic variant C/T snv 0.93 0.800 1.000 1 2011 2011
dbSNP: rs1477268
rs1477268
LINC01949 ; LOC101929380
1 5 87132049 intron variant T/C snv 0.23 0.700 1.000 1 2012 2012
dbSNP: rs16902538
rs16902538
LINC01949 ; LOC101929380
1 5 87121196 intron variant C/T snv 0.23 0.700 1.000 1 2012 2012
dbSNP: rs17591778
rs17591778
LINC01949 ; LOC101929380
1 5 87124575 intron variant G/A snv 0.25 0.700 1.000 1 2012 2012
dbSNP: rs17629700
rs17629700
LINC01949 ; LOC101929380
1 5 87124691 intron variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs17629760
rs17629760
LINC01949 ; LOC101929380
1 5 87128242 intron variant G/A snv 0.23 0.700 1.000 1 2012 2012
dbSNP: rs2544698
rs2544698
LOC101929380
1 5 87159014 intergenic variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs411174
rs411174
ITK
1 5 157181989 intron variant G/A snv 0.34 0.800 1.000 1 2011 2011
dbSNP: rs4141503
rs4141503
LINC01949 ; LOC101929380
1 5 87128859 intron variant C/T snv 0.23 0.700 1.000 1 2012 2012
dbSNP: rs10106540
rs10106540 		1 8 133449608 TF binding site variant A/G snv 0.38 0.800 1.000 1 2013 2013
dbSNP: rs2701448
rs2701448
TRPA1 ; MSC-AS1
1 8 72096014 intron variant C/A;T snv 8.2E-02 0.700 1.000 1 2013 2013
dbSNP: rs9650241
rs9650241
MSC-AS1
1 8 72115189 intron variant G/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs1394936
rs1394936 		1 9 78599117 intergenic variant T/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs1394937
rs1394937 		1 9 78587551 upstream gene variant G/C snv 0.73 0.700 1.000 1 2012 2012
dbSNP: rs1505634
rs1505634 		1 9 78594735 intergenic variant A/C;G;T snv 0.700 1.000 1 2012 2012