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: rs10096495
rs10096495
LOXL2 ; ENTPD4
1 8 23388270 intron variant C/T snv 8.7E-02 0.700 1.000 1 2013 2013
dbSNP: rs1010278
rs1010278 		1 8 57641227 intron variant A/C;T snv 0.700 1.000 1 2013 2013
dbSNP: rs10115200
rs10115200 		1 9 81451095 intergenic variant T/C snv 7.4E-02 0.700 1.000 1 2013 2013
dbSNP: rs1011685
rs1011685 		1 8 19973258 regulatory region variant C/T snv 8.7E-02 0.700 1.000 1 2012 2012
dbSNP: rs10118133
rs10118133
LOC101927502
1 9 81752279 intron variant A/G snv 0.46 0.700 1.000 1 2013 2013
dbSNP: rs10120450
rs10120450
PTPRD
1 9 8826588 intron variant T/C snv 0.58 0.700 1.000 1 2013 2013
dbSNP: rs10120501
rs10120501
PTPRD
1 9 8826767 intron variant T/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs10121203
rs10121203
PTPRD
1 9 8833227 intron variant A/C;G snv 0.700 1.000 1 2013 2013
dbSNP: rs10121993
rs10121993
PIP5K1B
1 9 68713462 intron variant G/A snv 0.70 0.700 1.000 1 2013 2013
dbSNP: rs10130589
rs10130589
LOC728755
1 14 27506611 intron variant G/C snv 0.39 0.700 1.000 1 2013 2013
dbSNP: rs10132646
rs10132646
LOC728755
1 14 27496715 intron variant T/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs10132835
rs10132835
LOC728755
1 14 27510351 intron variant A/T snv 0.39 0.700 1.000 1 2013 2013
dbSNP: rs10137892
rs10137892
LOC728755
1 14 27496260 intron variant G/A snv 0.43 0.700 1.000 1 2013 2013
dbSNP: rs10141869
rs10141869
LOC105370504
1 14 53665936 intron variant A/C snv 0.20 0.700 1.000 1 2013 2013
dbSNP: rs10144569
rs10144569
LOC728755
1 14 27503650 intron variant C/T snv 0.39 0.700 1.000 1 2013 2013
dbSNP: rs10144572
rs10144572
LOC728755
1 14 27503663 intron variant C/A;G snv 0.700 1.000 1 2013 2013
dbSNP: rs10149929
rs10149929 		1 14 98246151 intergenic variant G/A snv 0.31 0.700 1.000 1 2013 2013
dbSNP: rs10152202
rs10152202
LIPC ; ALDH1A2 ; LIPC-AS1
1 15 58452149 intron variant T/G snv 0.21 0.700 1.000 1 2012 2012
dbSNP: rs10152355
rs10152355
ALDH1A2
1 15 58378979 intron variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10157265
rs10157265
DOCK7
1 1 62627946 3 prime UTR variant C/T snv 0.43 0.700 1.000 1 2012 2012
dbSNP: rs10158897
rs10158897
USP1
1 1 62447248 intron variant C/T snv 0.33 0.700 1.000 1 2012 2012
dbSNP: rs10159255
rs10159255
DOCK7
1 1 62555145 intron variant C/A snv 0.36 0.700 1.000 1 2012 2012
dbSNP: rs10159528
rs10159528
GRID1
1 10 85725660 intron variant T/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs10159927
rs10159927 		1 10 8292500 intergenic variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs10162880
rs10162880
SHC4
1 15 48866901 intron variant G/A snv 0.56 0.700 1.000 1 2013 2013