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: rs145611121
rs145611121
PRDM16
1 1 3402268 intron variant -/C;CC delins 0.700 1.000 1 2016 2016
dbSNP: rs770551112
rs770551112
ZYG11A
1 1 52849688 intron variant -/CT;CTT ins 0.700 1.000 1 2016 2016
dbSNP: rs4953318
rs4953318
PRKCE
5 2 46127912 intron variant A/C snv 0.43 0.700 1.000 2 2012 2017
dbSNP: rs11654074
rs11654074
VMP1
5 17 59748211 intron variant A/C snv 0.40 0.700 1.000 1 2016 2016
dbSNP: rs2980853
rs2980853 		16 0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43 0.700 1.000 1 2016 2016
dbSNP: rs554093579
rs554093579 		1 7 100537063 upstream gene variant A/C snv 5.5E-03 0.700 1.000 1 2016 2016
dbSNP: rs115986297
rs115986297
GMDS
3 6 2050557 intron variant A/C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs1997595
rs1997595 		3 21 15205839 intron variant A/C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs11039436
rs11039436 		2 11 47866484 intergenic variant A/C;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs11065987
rs11065987 		17 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 0.800 1.000 2 2009 2017
dbSNP: rs833805
rs833805
LOC101929705
3 6 44062274 non coding transcript exon variant A/G snv 0.92 0.700 1.000 2 2016 2018
dbSNP: rs10224002
rs10224002
PRKAG2
12 0.925 0.080 7 151717955 intron variant A/G snv 0.31 0.800 1.000 1 2009 2009
dbSNP: rs10495928
rs10495928
PRKCE
5 2 46126027 intron variant A/G snv 0.36 0.700 1.000 1 2016 2016
dbSNP: rs11072566
rs11072566
NRG4
5 0.925 0.120 15 76001630 intron variant A/G snv 0.45 0.700 1.000 1 2017 2017
dbSNP: rs11072567
rs11072567
NRG4
5 15 76006403 intron variant A/G snv 0.43 0.700 1.000 1 2016 2016
dbSNP: rs11665867
rs11665867
SNRPA
1 19 40760574 intron variant A/G snv 0.13 0.700 1.000 1 2016 2016
dbSNP: rs11760376
rs11760376 		2 7 134684558 intron variant A/G snv 1.9E-03 0.700 1.000 1 2016 2016
dbSNP: rs12579302
rs12579302
ATP2B1
19 0.851 0.120 12 89656726 intron variant A/G snv 0.15 0.700 1.000 1 2016 2016
dbSNP: rs12889267
rs12889267
ARHGEF40
4 14 21074607 missense variant A/G snv 0.16 0.13 0.700 1.000 1 2016 2016
dbSNP: rs1340817
rs1340817 		2 13 28656444 upstream gene variant A/G snv 0.47 0.700 1.000 1 2016 2016
dbSNP: rs17563683
rs17563683
LINC02210-CRHR1 ; LOC107985028
3 17 45733706 intron variant A/G snv 0.15 0.700 1.000 1 2016 2016
dbSNP: rs17773190
rs17773190
LINC01118
3 2 46803224 intron variant A/G snv 0.32 0.700 1.000 1 2016 2016
dbSNP: rs1905376
rs1905376
TRPS1
2 8 115521531 intron variant A/G snv 0.55 0.700 1.000 1 2016 2016
dbSNP: rs2075672
rs2075672
TFR2 ; ACTL6B
8 7 100642673 intron variant A/G snv 0.65 0.700 1.000 1 2017 2017
dbSNP: rs261332
rs261332
LIPC ; ALDH1A2 ; LIPC-AS1
20 0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 0.700 1.000 1 2016 2016