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: rs2112347
rs2112347
POC5 ; LOC441087
10 0.925 0.120 5 75719417 upstream gene variant T/G snv 0.42 0.700 1.000 9 2010 2019
dbSNP: rs2270204
rs2270204
SWI5
1 9 128280455 intron variant T/G snv 0.41 0.700 1.000 4 2015 2018
dbSNP: rs4671328
rs4671328
LINC01122
1 2 58708147 intron variant T/G snv 0.56 0.700 1.000 4 2017 2019
dbSNP: rs7243357
rs7243357 		2 18 59216087 upstream gene variant T/G snv 0.18 0.700 1.000 4 2015 2019
dbSNP: rs13078960
rs13078960
CADM2
2 3 85758440 intron variant T/G snv 0.15 0.700 1.000 3 2015 2018
dbSNP: rs7024334
rs7024334
LINC01505
1 9 106309794 intron variant T/G snv 0.79 0.700 1.000 3 2017 2019
dbSNP: rs2237579
rs2237579
CALCR
1 7 93466555 intron variant T/G snv 0.40 0.700 1.000 2 2017 2018
dbSNP: rs4755726
rs4755726
HSD17B12
1 11 43620580 intron variant T/G snv 0.68 0.700 1.000 2 2015 2018
dbSNP: rs76594121
rs76594121
DNAJB8-AS1
1 3 128470548 intron variant T/G snv 3.0E-02 0.700 1.000 2 2019 2019
dbSNP: rs76895963
rs76895963
CCND2 ; CCND2-AS1
6 1.000 0.080 12 4275678 intron variant T/G snv 1.5E-02 0.700 1.000 2 2019 2019
dbSNP: rs7944782
rs7944782 		1 11 130925803 intergenic variant T/G snv 0.52 0.700 1.000 2 2019 2019
dbSNP: rs876424
rs876424
CPNE4
1 3 131918832 intron variant T/G snv 0.40 0.700 1.000 2 2015 2018
dbSNP: rs10192119
rs10192119
FIGN
1 2 163724731 intron variant T/G snv 0.28 0.700 1.000 1 2019 2019
dbSNP: rs1038088
rs1038088
SSH2
1 17 29747545 intron variant T/G snv 0.46 0.700 1.000 1 2019 2019
dbSNP: rs10513801
rs10513801
ETV5
3 3 186104564 intron variant T/G snv 9.2E-02 0.700 1.000 1 2019 2019
dbSNP: rs10767654
rs10767654
BDNF-AS ; LINC00678
2 11 27618676 intron variant T/G snv 0.73 0.700 1.000 1 2017 2017
dbSNP: rs10799778
rs10799778 		1 1 22986860 intergenic variant T/G snv 0.74 0.700 1.000 1 2019 2019
dbSNP: rs10861861
rs10861861 		1 12 108042619 intergenic variant T/G snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs10885122
rs10885122 		4 1.000 0.080 10 111282335 intergenic variant T/G snv 0.71 0.800 1.000 1 2012 2012
dbSNP: rs11047132
rs11047132
SOX5
1 12 23855501 intron variant T/G snv 9.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs11608710
rs11608710
SOX5
1 12 23600993 intron variant T/G snv 5.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs12229654
rs12229654 		20 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 0.700 1.000 1 2014 2014
dbSNP: rs12522567
rs12522567
CWC27
1 5 64791196 intron variant T/G snv 0.51 0.700 1.000 1 2019 2019
dbSNP: rs12716979
rs12716979
STX1B
1 16 31000500 intron variant T/G snv 0.35 0.700 1.000 1 2019 2019
dbSNP: rs12890931
rs12890931
GALNT16
1 14 69286652 intron variant T/G snv 0.42 0.700 1.000 1 2019 2019