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: rs1487022
rs1487022
VPS13B
2 0.925 0.120 8 99517598 intron variant G/T snv 0.17 0.700 1.000 1 2017 2017
dbSNP: rs150382487
rs150382487
LINC02476
1 1.000 0.120 7 119500548 intron variant T/A snv 2.4E-03 0.700 1.000 1 2019 2019
dbSNP: rs1528845
rs1528845 		1 1.000 0.120 2 147749295 intergenic variant T/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs1588366
rs1588366
TANC2
2 0.925 0.120 17 62999067 regulatory region variant A/G snv 0.23 0.700 1.000 1 2017 2017
dbSNP: rs1688766
rs1688766
FILIP1L ; CMSS1
2 0.925 0.120 3 99929006 intron variant G/A snv 0.18 0.700 1.000 1 2017 2017
dbSNP: rs182830500
rs182830500
LINC02476
1 1.000 0.120 7 119521299 intron variant T/C snv 2.6E-03 0.700 1.000 1 2019 2019
dbSNP: rs1838105
rs1838105
GOSR2 ; LRRC37A2
2 0.925 0.120 17 46931569 non coding transcript exon variant A/G snv 0.63 0.700 1.000 1 2017 2017
dbSNP: rs1873147
rs1873147 		2 0.925 0.120 15 63020433 regulatory region variant G/A snv 0.66 0.700 1.000 1 2018 2018
dbSNP: rs1878918
rs1878918
NRG1
2 0.925 0.120 8 32476054 intron variant G/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs188681640
rs188681640
LINC02476
1 1.000 0.120 7 119506105 intron variant A/G snv 2.4E-03 0.700 1.000 1 2019 2019
dbSNP: rs189675673
rs189675673
SULT2A1
1 1.000 0.120 19 47880143 intron variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1907989
rs1907989 		2 0.925 0.120 4 4817198 upstream gene variant A/G snv 0.36 0.700 1.000 1 2017 2017
dbSNP: rs2006771
rs2006771
SFI1
2 0.925 0.120 22 31602626 missense variant G/A snv 0.41 0.44 0.700 1.000 1 2017 2017
dbSNP: rs2064163
rs2064163 		2 0.925 0.120 1 209875474 regulatory region variant G/T snv 0.30 0.700 1.000 1 2017 2017
dbSNP: rs2073764
rs2073764
GNB1L
2 0.925 0.120 22 19811887 intron variant C/T snv 6.0E-03 0.700 1.000 1 2017 2017
dbSNP: rs2283487
rs2283487 		2 0.925 0.120 16 3919885 intergenic variant A/C;G snv 0.700 1.000 1 2017 2017
dbSNP: rs2289187
rs2289187
UBL7
2 0.925 0.120 15 74452058 intron variant C/T snv 0.24 0.700 1.000 1 2017 2017
dbSNP: rs2304269
rs2304269
TMEM19
2 0.925 0.120 12 71686492 5 prime UTR variant T/C snv 6.5E-02 0.700 1.000 1 2017 2017
dbSNP: rs2325377
rs2325377 		1 1.000 0.120 13 71321166 intergenic variant C/T snv 0.99 0.700 1.000 1 2019 2019
dbSNP: rs2363632
rs2363632 		2 0.925 0.120 12 52963551 intergenic variant T/G snv 7.7E-02 0.700 1.000 1 2017 2017
dbSNP: rs2405373
rs2405373
LOC105376157
1 1.000 0.120 9 95549844 intergenic variant G/A snv 0.32 0.700 1.000 1 2019 2019
dbSNP: rs28434654
rs28434654
LOC105376157
1 1.000 0.120 9 95524196 intergenic variant A/G snv 0.28 0.700 1.000 1 2019 2019
dbSNP: rs28637199
rs28637199
LOC105376157
1 1.000 0.120 9 95532166 intergenic variant T/G snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs28689133
rs28689133
LOC105376157
1 1.000 0.120 9 95531283 intergenic variant A/C;G snv 0.28 0.700 1.000 1 2019 2019
dbSNP: rs2872615
rs2872615 		2 0.925 0.120 17 9011376 intergenic variant T/C snv 0.23 0.700 1.000 1 2017 2017