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: rs12773465
rs12773465
SLIT1
2 10 97034302 intron variant A/G snv 0.12 0.700 1.000 1 2013 2013
dbSNP: rs1330225
rs1330225 		3 1 106293321 intergenic variant T/C snv 0.38 0.700 1.000 1 2013 2013
dbSNP: rs16849553
rs16849553
LINC02815 ; LINC02814
2 1 229201099 intron variant T/C snv 3.7E-02 0.700 1.000 1 2013 2013
dbSNP: rs16890334
rs16890334 		3 6 78846449 intergenic variant T/C snv 1.9E-03 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: rs17669622
rs17669622
ESRRG
2 1 216583479 intron variant G/A snv 0.18 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: rs2627282
rs2627282
LOC105377786
3 8 2923434 upstream gene variant G/A snv 0.25 0.700 1.000 1 2013 2013
dbSNP: rs3824755
rs3824755
CYP17A1
5 0.925 0.120 10 102836092 intron variant G/A;C;T snv 0.700 1.000 1 2013 2013
dbSNP: rs4537030
rs4537030 		2 5 7243868 downstream gene variant T/G snv 0.31 0.700 1.000 1 2013 2013
dbSNP: rs7577262
rs7577262 		4 2 233910224 intergenic variant G/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs7791745
rs7791745 		2 7 42345021 regulatory region variant T/C snv 0.73 0.700 1.000 1 2013 2013
dbSNP: rs9874923
rs9874923
KAT2B
2 3 20060071 intron variant C/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs12195036
rs12195036
LOC105378117
2 6 166038209 intergenic variant T/C snv 4.1E-02 0.700 1.000 1 2014 2014
dbSNP: rs12416687
rs12416687
AS3MT ; BORCS7-ASMT
2 10 102869254 intron variant T/C snv 0.21 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: rs4841895
rs4841895
LOC100506532
2 9 134532196 intron variant G/A snv 0.32 0.700 1.000 1 2014 2014
dbSNP: rs4842666
rs4842666 		3 12 89547772 non coding transcript exon variant T/C snv 0.16 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: rs747685
rs747685
NXN
2 17 871811 intron variant T/A snv 0.12 0.700 1.000 1 2014 2014
dbSNP: rs604723
rs604723
ARHGAP42
9 1.000 0.040 11 100739815 intron variant T/C snv 0.78 0.700 1.000 3 2015 2018
dbSNP: rs1275988
rs1275988
KCNK3
6 1.000 0.080 2 26691496 upstream gene variant C/T snv 0.48 0.700 1.000 2 2015 2018
dbSNP: rs13149993
rs13149993 		6 4 80237391 regulatory region variant G/A;C snv 0.700 1.000 2 2015 2018