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: rs1448817
rs1448817 		1 1.000 0.080 4 110719897 intergenic variant A/G snv 0.37 0.700 1.000 2 2007 2009
dbSNP: rs146518726
rs146518726 		1 1.000 0.080 1 51069367 intergenic variant G/A snv 1.8E-02 0.700 1.000 2 2018 2018
dbSNP: rs1957021
rs1957021
AKAP6
1 1.000 0.080 14 32455299 intron variant T/A;C snv 0.700 1.000 2 2018 2018
dbSNP: rs2012809
rs2012809
SLC27A6 ; LOC105379168
1 1.000 0.080 5 128854670 intron variant A/G snv 0.86 0.700 1.000 2 2018 2018
dbSNP: rs2129977
rs2129977 		1 1.000 0.080 4 110791276 upstream gene variant A/G;T snv 0.700 1.000 2 2017 2018
dbSNP: rs2359171
rs2359171
ZFHX3
1 1.000 0.080 16 73019123 intron variant T/A snv 0.21 0.700 1.000 2 2018 2018
dbSNP: rs2723064
rs2723064
LINC02245 ; LINC02576 ; LOC107984063
1 1.000 0.080 2 65052671 non coding transcript exon variant T/C snv 0.40 0.700 1.000 2 2017 2018
dbSNP: rs2738413
rs2738413
ESR2 ; SYNE2
1 1.000 0.080 14 64213242 intron variant A/G snv 0.63 0.700 1.000 2 2018 2018
dbSNP: rs2834618
rs2834618
LINC01426
1 1.000 0.080 21 34746814 intron variant T/G snv 9.5E-02 0.700 1.000 2 2018 2018
dbSNP: rs2860482
rs2860482
NACA
1 1.000 0.080 12 56712154 downstream gene variant A/C snv 0.80 0.700 1.000 2 2018 2018
dbSNP: rs2885697
rs2885697
SCMH1
2 1.000 0.080 1 41078607 intron variant G/T snv 0.72 0.700 1.000 2 2018 2018
dbSNP: rs3176326
rs3176326
CDKN1A ; DINOL
1 1.000 0.080 6 36679512 intron variant G/A snv 0.20 0.700 1.000 2 2018 2018
dbSNP: rs34969716
rs34969716
KDM1B
1 1.000 0.080 6 18209878 intron variant G/A snv 0.24 0.700 1.000 2 2018 2018
dbSNP: rs35620480
rs35620480
LOC105379242
1 1.000 0.080 8 11642399 upstream gene variant A/C snv 0.11 0.700 1.000 2 2018 2018
dbSNP: rs4871397
rs4871397 		1 1.000 0.080 8 123622957 intron variant G/C;T snv 0.700 1.000 2 2018 2018
dbSNP: rs4999127
rs4999127
KCNN3
1 1.000 0.080 1 154741530 intron variant G/A snv 0.89 0.700 1.000 2 2018 2018
dbSNP: rs55734480
rs55734480
DGKB
1 1.000 0.080 7 14332384 intron variant G/A snv 0.20 0.700 1.000 2 2018 2018
dbSNP: rs55985730
rs55985730
OPN1SW
1 1.000 0.080 7 128776990 upstream gene variant T/G snv 4.1E-02 0.700 1.000 2 2018 2018
dbSNP: rs56181519
rs56181519 		1 1.000 0.080 2 174690986 intron variant C/T snv 0.27 0.700 1.000 2 2018 2018
dbSNP: rs577676
rs577676 		1 1.000 0.080 1 170618199 intron variant C/T snv 0.56 0.700 1.000 2 2017 2018
dbSNP: rs60212594
rs60212594
SYNPO2L ; LOC105378360
1 1.000 0.080 10 73654586 intron variant G/A;C snv 0.15 0.700 1.000 2 2018 2018
dbSNP: rs60572254
rs60572254
NEURL1
1 1.000 0.080 10 103565017 intron variant C/T snv 0.700 1.000 2 2017 2018
dbSNP: rs60902112
rs60902112
XXYLT1
1 1.000 0.080 3 195080124 intron variant C/T snv 0.27 0.700 1.000 2 2018 2018
dbSNP: rs62521286
rs62521286
FBXO32
2 1.000 0.080 8 123539735 intron variant A/G snv 6.6E-02 0.700 1.000 2 2018 2018
dbSNP: rs6790396
rs6790396
SCN10A
3 1.000 0.080 3 38730434 intron variant C/G snv 0.67 0.700 1.000 2 2018 2018