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: rs1419856
rs1419856 		1 7 35267372 intergenic variant A/G snv 0.11 0.700 1.000 1 2016 2016
dbSNP: rs1562782
rs1562782
AMPD3 ; CAND1.11
1 11 10321164 intron variant A/C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs17020136
rs17020136
HEATR5B
2 2 37020872 intron variant T/C snv 0.24 0.18 0.700 1.000 1 2016 2016
dbSNP: rs17391905
rs17391905 		2 1 51080468 intergenic variant T/G snv 3.7E-02 0.700 1.000 1 2016 2016
dbSNP: rs174577
rs174577
FADS2
13 1.000 0.080 11 61837342 intron variant C/A snv 0.38 0.700 1.000 1 2016 2016
dbSNP: rs17608766
rs17608766
GOSR2 ; LRRC37A2
8 1.000 0.040 17 46935905 3 prime UTR variant T/C snv 9.2E-02 0.700 1.000 1 2016 2016
dbSNP: rs1886512
rs1886512
KLF12
2 13 73946049 intron variant T/A snv 0.40 0.700 1.000 1 2016 2016
dbSNP: rs1991601
rs1991601
WIPF1
1 2 174603041 intron variant T/C snv 0.79 0.700 1.000 1 2016 2016
dbSNP: rs2025096
rs2025096
GSS
3 20 34952197 5 prime UTR variant G/A snv 0.19 0.700 1.000 1 2016 2016
dbSNP: rs2051211
rs2051211
EXOG
1 3 38518258 intron variant A/C;G snv 0.23 0.700 1.000 1 2016 2016
dbSNP: rs2207790
rs2207790
NFIA
1 1 61432295 intron variant G/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs2242285
rs2242285
LRIG1 ; SLC25A26
2 3 66381178 intron variant A/C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs242562
rs242562
MAPT
2 1.000 0.040 17 45949373 intron variant G/A snv 0.35 0.700 1.000 1 2016 2016
dbSNP: rs2997447
rs2997447
TRIM63
1 1 26060932 intron variant G/A snv 0.24 0.700 1.000 1 2016 2016
dbSNP: rs359466
rs359466
CPEB4
1 5 173888863 5 prime UTR variant C/G snv 0.11 0.700 1.000 1 2016 2016
dbSNP: rs3770770
rs3770770
STRN
1 2 36965723 intron variant C/T snv 0.18 0.700 1.000 1 2016 2016
dbSNP: rs3777755
rs3777755
HIVEP1
1 6 12159466 intron variant C/T snv 0.23 0.700 1.000 1 2016 2016
dbSNP: rs3929778
rs3929778
CASC20
1 20 6479643 intron variant C/T snv 0.84 0.700 1.000 1 2016 2016
dbSNP: rs4074536
rs4074536
CASQ2
2 1 115768346 missense variant T/C snv 0.33 0.34 0.700 1.000 1 2016 2016
dbSNP: rs4642101
rs4642101
CAND2
3 1.000 0.080 3 12800724 intron variant T/G snv 0.63 0.700 1.000 1 2016 2016
dbSNP: rs4687718
rs4687718
TKT
2 3 53248287 intron variant A/G snv 0.75 0.700 1.000 1 2016 2016
dbSNP: rs4708832
rs4708832 		1 6 159472905 intron variant G/T snv 0.31 0.700 1.000 1 2016 2016
dbSNP: rs6683273
rs6683273
PRDM16
1 1 3342619 intron variant A/G snv 6.8E-02 0.700 1.000 1 2016 2016
dbSNP: rs6801957
rs6801957
SCN10A
7 1.000 0.080 3 38725824 intron variant T/C snv 0.67 0.700 1.000 1 2016 2016
dbSNP: rs6968945
rs6968945 		1 7 46601302 intergenic variant C/T snv 0.61 0.700 1.000 1 2016 2016