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: rs145471199
rs145471199 		1 7 9407441 intergenic variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs147828834
rs147828834
FSIP1
1 15 39602982 intron variant A/T snv 8.3E-03 0.700 1.000 1 2018 2018
dbSNP: rs147906088
rs147906088 		2 1.000 0.080 7 54496119 intergenic variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs148410317
rs148410317
IFITM10
1 11 1749985 intron variant G/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs150900094
rs150900094 		1 15 87284961 intergenic variant A/C snv 2.9E-02 0.700 1.000 1 2018 2018
dbSNP: rs157582
rs157582
TOMM40
8 0.851 0.160 19 44892962 intron variant C/T snv 0.24 0.29 0.700 1.000 1 2017 2017
dbSNP: rs16873450
rs16873450
STK31
1 7 23767021 intron variant A/G snv 0.55 0.700 1.000 1 2017 2017
dbSNP: rs16986890
rs16986890
CTNNBL1
1 20 37698121 intron variant A/G snv 9.3E-02 0.700 1.000 1 2013 2013
dbSNP: rs28715237
rs28715237
LINC00334
1 21 45253853 intron variant C/G snv 0.700 1.000 1 2018 2018
dbSNP: rs2976464
rs2976464
ZNF250
2 1.000 0.040 8 144902955 upstream gene variant A/G snv 0.46 0.700 1.000 1 2018 2018
dbSNP: rs34454929
rs34454929
KCNE4
1 2 223083837 intron variant T/C snv 3.2E-02 0.700 1.000 1 2018 2018
dbSNP: rs35551159
rs35551159 		1 12 60075450 intergenic variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs3801203
rs3801203
GLI3
1 7 42148801 intron variant C/A snv 0.13 0.700 1.000 1 2017 2017
dbSNP: rs429358
rs429358
APOE
66 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 0.700 1.000 1 2018 2018
dbSNP: rs4420638
rs4420638
APOC1
43 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 0.700 1.000 1 2015 2015
dbSNP: rs4762194
rs4762194 		1 12 97789941 intergenic variant G/A snv 0.20 0.700 1.000 1 2018 2018
dbSNP: rs4776997
rs4776997 		1 15 67858585 intron variant A/G;T snv 0.77 0.700 1.000 1 2015 2015
dbSNP: rs4942792
rs4942792
PDS5B
1 13 32663326 intron variant C/A;G snv 0.700 1.000 1 2018 2018
dbSNP: rs56186534
rs56186534
LOC105369949
1 12 104410836 regulatory region variant G/C snv 5.0E-02 0.700 1.000 1 2018 2018
dbSNP: rs56214552
rs56214552
TRIQK
2 1.000 0.080 8 93011994 intron variant T/G snv 0.24 0.700 1.000 1 2018 2018
dbSNP: rs56353579
rs56353579
GOLM1
1 9 86078634 intron variant G/A snv 1.9E-02 0.700 1.000 1 2018 2018
dbSNP: rs5747035
rs5747035
ADA2
1 22 17237716 intron variant T/C snv 0.15 0.700 1.000 1 2015 2015
dbSNP: rs6012770
rs6012770
LOC100287792
1 20 37675713 upstream gene variant G/A snv 9.6E-02 0.700 1.000 1 2013 2013
dbSNP: rs6020113
rs6020113 		1 20 37674643 upstream gene variant G/A snv 9.2E-02 0.700 1.000 1 2013 2013
dbSNP: rs6020395
rs6020395
CTNNBL1
1 20 37710922 intron variant G/C snv 0.16 0.700 1.000 1 2013 2013