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: rs11205
rs11205
HSD17B4
1 1.000 0.120 5 119526018 missense variant A/G snv 0.42 0.41 0.010 1.000 1 2010 2010
dbSNP: rs11769858
rs11769858 		1 1.000 0.120 7 158708801 upstream gene variant T/C snv 0.60 0.700 1.000 1 2017 2017
dbSNP: rs12228415
rs12228415
ATF7IP
1 1.000 0.120 12 14367767 intron variant A/G snv 0.41 0.010 1.000 1 2017 2017
dbSNP: rs12434245
rs12434245
ESR2 ; SYNE2
1 1.000 0.120 14 64225135 intron variant C/T snv 5.6E-02 0.010 1.000 1 2012 2012
dbSNP: rs12481572
rs12481572
ZFP64 ; LOC105372664
1 1.000 0.120 20 52091515 intron variant A/T snv 0.17 0.700 1.000 1 2017 2017
dbSNP: rs1267543
rs1267543
TEX14 ; LOC107985048
1 1.000 0.120 17 58579263 intron variant A/G snv 0.78 0.700 1.000 1 2013 2013
dbSNP: rs12912292
rs12912292 		1 1.000 0.120 15 55746509 upstream gene variant G/A snv 0.36 0.700 1.000 1 2017 2017
dbSNP: rs1355972653
rs1355972653
IFNGR2
3 0.882 0.120 21 33415009 synonymous variant G/A snv 4.0E-06 7.0E-06 0.010 1.000 1 2007 2007
dbSNP: rs17153755
rs17153755
GATA4
1 1.000 0.120 8 11753991 intron variant C/G snv 0.34 0.700 1.000 1 2017 2017
dbSNP: rs17198432
rs17198432 		1 1.000 0.120 2 175524333 intergenic variant C/A snv 8.9E-02 0.010 1.000 1 2019 2019
dbSNP: rs17336718
rs17336718
TKTL1
1 1.000 0.120 X 154307767 intron variant C/T snv 4.8E-02 0.700 1.000 1 2017 2017
dbSNP: rs17689040
rs17689040
LOC105375242
1 1.000 0.120 7 40880714 intergenic variant C/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs2075789
rs2075789
MSH5 ; MSH5-SAPCD1 ; LOC105375020
6 0.882 0.120 6 31740551 missense variant C/T snv 0.13 9.1E-02 0.010 1.000 1 2016 2016
dbSNP: rs2241024
rs2241024
LINC00662
1 1.000 0.120 19 27766485 intron variant G/A snv 0.15 0.700 1.000 1 2017 2017
dbSNP: rs2414099
rs2414099
CYP19A1 ; MIR4713HG
1 1.000 0.120 15 51256585 intron variant C/T snv 0.83 0.010 1.000 1 2012 2012
dbSNP: rs2713206
rs2713206
TFCP2L1
1 1.000 0.120 2 121250365 intron variant C/T snv 0.21 0.700 1.000 1 2017 2017
dbSNP: rs34601376
rs34601376 		1 1.000 0.120 19 23868026 intron variant A/T snv 0.14 0.700 1.000 1 2017 2017
dbSNP: rs3755605
rs3755605
GPR160
1 1.000 0.120 3 170038331 non coding transcript exon variant C/T snv 0.46 0.700 1.000 1 2017 2017
dbSNP: rs3778991
rs3778991
MAD1L1
1 1.000 0.120 7 2132820 intron variant G/A snv 0.27 0.700 1.000 1 2013 2013
dbSNP: rs3805663
rs3805663
PITX1
2 1.000 0.120 5 135030510 intron variant A/G snv 0.49 0.700 1.000 1 2013 2013
dbSNP: rs4240895
rs4240895
PIK3CD ; PIK3CD-AS1
1 1.000 0.120 1 9653328 non coding transcript exon variant C/T snv 0.53 0.700 1.000 1 2017 2017
dbSNP: rs4471514
rs4471514
VEZT
1 1.000 0.120 12 95273561 intron variant C/T snv 0.48 0.010 1.000 1 2012 2012
dbSNP: rs4599029
rs4599029 		1 1.000 0.120 19 53781435 intergenic variant G/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs4862848
rs4862848
ZFP42
1 1.000 0.120 4 188000286 intron variant A/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs4931000
rs4931000
RESF1
1 1.000 0.120 12 31988561 intron variant A/G snv 0.78 0.700 1.000 1 2017 2017