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: rs1330225
rs1330225 		3 1 106293321 intergenic variant T/C snv 0.38 0.700 1.000 1 2013 2013
dbSNP: rs1401454
rs1401454
SOX6
3 11 16228637 intron variant C/A;G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs17135875
rs17135875
FBXL13
3 7 102878584 intron variant T/C snv 0.24 0.700 1.000 1 2013 2013
dbSNP: rs1943940
rs1943940 		3 18 74037957 upstream gene variant T/C snv 0.42 0.700 1.000 1 2013 2013
dbSNP: rs2030114
rs2030114
HNRNPA1P48
2 16 51576036 intron variant G/A snv 0.23 0.700 1.000 1 2013 2013
dbSNP: rs2627282
rs2627282
LOC105377786
3 8 2923434 upstream gene variant G/A snv 0.25 0.700 1.000 1 2013 2013
dbSNP: rs6924906
rs6924906
TENT5A ; LOC105377871
2 6 81510835 intron variant T/C snv 0.12 0.700 1.000 1 2013 2013
dbSNP: rs7286472
rs7286472 		2 22 33990484 intergenic variant A/G snv 0.19 0.700 1.000 1 2013 2013
dbSNP: rs7902871
rs7902871
SLIT1
2 10 97049946 intron variant A/G snv 0.21 0.700 1.000 1 2013 2013
dbSNP: rs9318552
rs9318552
OBI1-AS1
2 13 78451652 intron variant C/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs13390641
rs13390641 		3 2 103419975 intergenic variant G/A snv 0.12 0.700 1.000 1 2014 2014
dbSNP: rs16833934
rs16833934 		3 3 164019462 intergenic variant A/G snv 0.34 0.700 1.000 1 2014 2014
dbSNP: rs3118867
rs3118867
DAPK1
3 9 87646780 intron variant A/G snv 0.41 0.700 1.000 1 2014 2014
dbSNP: rs4601790
rs4601790
EHBP1L1
4 11 65586435 intron variant A/G snv 0.23 0.700 1.000 1 2014 2014
dbSNP: rs4638749
rs4638749 		2 2 108267586 downstream gene variant G/A snv 0.26 0.700 1.000 1 2014 2014
dbSNP: rs603788
rs603788
KCNMA1
3 10 77451504 intron variant G/C snv 0.46 0.700 1.000 1 2014 2014
dbSNP: rs747687
rs747687
NXN
2 17 872094 intron variant G/C snv 0.12 0.700 1.000 1 2014 2014
dbSNP: rs12579720
rs12579720
LINC02398
2 12 20020830 intron variant C/A;G;T snv 0.700 1.000 4 2015 2018
dbSNP: rs1887320
rs1887320 		6 20 10985350 intron variant G/A snv 0.46 0.700 1.000 3 2015 2018
dbSNP: rs1902859
rs1902859 		4 4 80236549 regulatory region variant T/C snv 0.27 0.700 1.000 3 2015 2019
dbSNP: rs11067763
rs11067763
LOC105370003
3 12 115760536 intron variant A/G snv 0.16 0.700 1.000 2 2015 2017
dbSNP: rs4409766
rs4409766
BORCS7 ; BORCS7-ASMT
6 1.000 0.040 10 102856906 intron variant T/C snv 0.14 0.700 1.000 2 2015 2017
dbSNP: rs4757391
rs4757391
SOX6
2 11 16281393 intron variant C/T snv 0.78 0.700 1.000 2 2015 2017
dbSNP: rs9687065
rs9687065
SH3TC2
2 5 149011577 intron variant A/G snv 0.17 0.700 1.000 2 2015 2017
dbSNP: rs9810888
rs9810888
CACNA1D
3 3 53601568 intron variant T/G snv 0.51 0.700 1.000 2 2015 2018