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: rs1996928
rs1996928
LINC01524 ; LOC105372666
1 20 52644875 intron variant G/A snv 0.27 0.700 1.000 1 2019 2019
dbSNP: rs2273640
rs2273640
BTBD7 ; UNC79
1 14 93332875 synonymous variant G/A snv 0.22 0.16 0.700 1.000 1 2018 2018
dbSNP: rs2393831
rs2393831
CABCOCO1
1 10 61706996 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs2422137
rs2422137
NEGR1
1 1 72154278 intron variant C/A snv 0.37 0.700 1.000 1 2019 2019
dbSNP: rs2472297
rs2472297 		9 0.882 0.160 15 74735539 intergenic variant C/T snv 0.16 0.700 1.000 1 2019 2019
dbSNP: rs2504671
rs2504671 		1 6 51340779 intergenic variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs2567241
rs2567241
CLGN
4 4 140402008 missense variant C/A snv 5.2E-02 6.0E-02 0.700 1.000 1 2016 2016
dbSNP: rs2761589
rs2761589
DCDC1
1 11 31289882 intron variant C/A;G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs2945091
rs2945091
LINC02742
1 11 28824022 intron variant G/A snv 0.45 0.700 1.000 1 2019 2019
dbSNP: rs2968426
rs2968426
GSE1 ; LOC107984830
1 16 85302129 intron variant G/C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs2984348
rs2984348
CITED1 ; LOC105373250
2 X 72308510 intron variant C/T snv 0.31 0.700 1.000 1 2018 2018
dbSNP: rs33951980
rs33951980
MLXIPL
3 7 73615107 intron variant C/T snv 0.10 0.700 1.000 1 2019 2019
dbSNP: rs34452566
rs34452566 		1 11 27771923 intron variant G/T snv 0.14 0.700 1.000 1 2019 2019
dbSNP: rs34562254
rs34562254
TNFRSF13B
3 1.000 0.160 17 16939677 missense variant G/A snv 0.14 0.12 0.700 1.000 1 2018 2018
dbSNP: rs34783010
rs34783010
GIPR
1 19 45677156 intron variant G/T snv 0.18 0.17 0.700 1.000 1 2019 2019
dbSNP: rs35397826
rs35397826
SLC16A6 ; ARSG
2 17 68273941 missense variant A/G snv 0.12 0.11 0.700 1.000 1 2018 2018
dbSNP: rs35487869
rs35487869
WDR72
1 15 53639111 intron variant C/A snv 0.34 0.700 1.000 1 2018 2018
dbSNP: rs39999
rs39999
NFAT5
1 16 69619793 intron variant C/G snv 0.89 0.700 1.000 1 2018 2018
dbSNP: rs40465
rs40465
LOC105379109
2 1.000 0.040 5 104646025 intron variant T/G snv 0.24 0.700 1.000 1 2019 2019
dbSNP: rs4410790
rs4410790
AHR ; LOC101927609
9 0.882 0.160 7 17244953 intron variant T/C snv 0.54 0.700 1.000 1 2019 2019
dbSNP: rs4442732
rs4442732 		1 14 60558899 downstream gene variant A/G snv 0.47 0.700 1.000 1 2019 2019
dbSNP: rs4664048
rs4664048
SLC4A10
1 2 161725744 intron variant A/T snv 0.83 0.700 1.000 1 2018 2018
dbSNP: rs4788415
rs4788415
ZNF771 ; DCTPP1
1 16 30427988 intron variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs4919683
rs4919683
WBP1L
1 10 102825368 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs55807911
rs55807911
BABAM2 ; LOC100505736
1 2 28198606 intron variant T/C snv 0.19 0.700 1.000 1 2019 2019