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: rs59876823
rs59876823
PCCA-DT
2 13 100082270 intron variant C/A snv 0.10 0.700 1.000 1 2015 2015
dbSNP: rs12588659
rs12588659
EVL
1 14 100121476 intron variant C/A snv 6.6E-02 0.700 1.000 1 2010 2010
dbSNP: rs10958852
rs10958852
PTPRD
2 9 10060843 intron variant C/T snv 4.5E-04 0.700 1.000 1 2015 2015
dbSNP: rs182466621
rs182466621
LOC105375310
2 2 100730839 intergenic variant G/A;T snv 0.700 1.000 1 2015 2015
dbSNP: rs140386998
rs140386998 		2 X 100959983 downstream gene variant C/T snv 3.7E-02 0.700 1.000 1 2015 2015
dbSNP: rs60866311
rs60866311
NPAS2 ; NPAS2-AS1
2 2 100975599 non coding transcript exon variant T/G snv 4.1E-02 7.2E-02 0.700 1.000 1 2015 2015
dbSNP: rs17396340
rs17396340
KIF1B
3 1 10226118 intron variant G/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs3862030
rs3862030
SUFU
2 10 102567827 intron variant A/G snv 0.45 0.700 1.000 1 2017 2017
dbSNP: rs7917772
rs7917772
SFXN2
3 10 102727686 3 prime UTR variant G/A;C snv 0.46 0.700 1.000 1 2017 2017
dbSNP: rs71417845
rs71417845 		2 14 103210903 downstream gene variant C/G snv 1.7E-02 0.700 1.000 1 2015 2015
dbSNP: rs41427747
rs41427747
LINC02503
2 4 103999322 intron variant G/T snv 5.6E-02 0.700 1.000 1 2015 2015
dbSNP: rs395962
rs395962
LIN28B
6 6 104949543 intron variant T/G snv 0.72 0.700 1.000 1 2017 2017
dbSNP: rs10991437
rs10991437
CT70
2 9 104973639 intron variant C/A snv 9.0E-02 0.700 1.000 1 2017 2017
dbSNP: rs58376408
rs58376408 		2 16 10504450 regulatory region variant C/G snv 6.5E-02 0.700 1.000 1 2015 2015
dbSNP: rs144529734
rs144529734
LOC107984266
2 10 105647558 intergenic variant G/T snv 1.4E-02 0.700 1.000 1 2015 2015
dbSNP: rs9408815
rs9408815
LINC01505
2 9 106128240 intron variant C/G snv 0.20 0.700 1.000 1 2017 2017
dbSNP: rs9409082
rs9409082
LINC01505
2 9 106138768 intron variant C/T snv 0.20 0.700 1.000 1 2017 2017
dbSNP: rs670752
rs670752
BBX
2 3 107594133 intron variant G/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs13271456
rs13271456
PINX1 ; LOC102723313
2 8 10767736 intron variant G/A snv 2.7E-02 0.700 1.000 1 2015 2015
dbSNP: rs6437740
rs6437740
BBX
2 3 107746970 intron variant T/C snv 0.25 0.700 1.000 1 2009 2009
dbSNP: rs12710258
rs12710258
CARM1
2 19 10879653 intron variant C/T snv 0.16 0.700 1.000 1 2015 2015
dbSNP: rs10041657
rs10041657
FER
2 5 108816727 intron variant G/A snv 0.23 0.700 1.000 1 2017 2017
dbSNP: rs78553789
rs78553789
MYO16
2 13 108904171 intron variant T/C snv 2.3E-02 0.700 1.000 1 2015 2015
dbSNP: rs848353
rs848353 		3 1.000 0.080 7 108908603 upstream gene variant A/G snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs117178387
rs117178387
AMD1 ; CDK19
2 6 110815877 non coding transcript exon variant T/C snv 3.2E-02 0.700 1.000 1 2015 2015