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: rs10007186
rs10007186
LINC01094
2 4 78667891 intron variant C/T snv 0.65 0.700 1.000 1 2012 2012
dbSNP: rs1000778
rs1000778
FADS3
3 1.000 0.040 11 61887833 intron variant A/G snv 0.59 0.700 1.000 1 2012 2012
dbSNP: rs1001159
rs1001159 		1 9 36728588 intergenic variant C/T snv 0.56 0.700 1.000 1 2013 2013
dbSNP: rs10018448
rs10018448
PPM1K-DT
1 4 88304019 intron variant A/G snv 0.58 0.700 1.000 1 2012 2012
dbSNP: rs10024717
rs10024717
PPM1K-DT
1 4 88298493 intron variant G/A snv 0.29 0.700 1.000 1 2012 2012
dbSNP: rs1002475
rs1002475
REV3L ; MFSD4B
1 6 111388386 intron variant T/C snv 0.39 0.700 1.000 1 2012 2012
dbSNP: rs1002687
rs1002687
DOCK7
1 1 62498066 intron variant G/A snv 0.57 0.700 1.000 1 2012 2012
dbSNP: rs10057473
rs10057473 		1 5 143507813 intron variant G/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs1007205
rs1007205
DOCK7
1 1 62471241 intron variant T/A;C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs1007995
rs1007995
LOC101927502
1 9 81757012 intron variant A/G snv 0.46 0.700 1.000 1 2013 2013
dbSNP: rs10095723
rs10095723
LOXL2 ; ENTPD4
1 8 23385810 3 prime UTR variant T/C snv 8.0E-02 0.700 1.000 1 2013 2013
dbSNP: rs10096495
rs10096495
LOXL2 ; ENTPD4
1 8 23388270 intron variant C/T snv 8.7E-02 0.700 1.000 1 2013 2013
dbSNP: rs10096633
rs10096633 		8 1.000 0.040 8 19973410 regulatory region variant C/T snv 0.22 0.700 1.000 1 2012 2012
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