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: rs16849225
rs16849225 		5 2 164050310 intron variant C/T snv 0.19 0.700 1.000 4 2011 2018
dbSNP: rs419076
rs419076
MECOM
6 3 169383098 intron variant T/A;C snv 0.700 1.000 4 2011 2018
dbSNP: rs6015450
rs6015450
ZNF831
7 20 59176062 intron variant A/G snv 0.14 0.700 1.000 4 2011 2018
dbSNP: rs932764
rs932764
PLCE1
6 10 94136183 intron variant A/G snv 0.38 0.700 1.000 4 2011 2017
dbSNP: rs11066280
rs11066280
HECTD4
27 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 0.700 1.000 3 2011 2015
dbSNP: rs1173766
rs1173766 		5 5 32804422 intergenic variant T/C snv 0.57 0.700 1.000 3 2011 2018
dbSNP: rs2932538
rs2932538
MOV10
4 1 112673921 intron variant A/C;G snv 0.700 1.000 3 2011 2017
dbSNP: rs7129220
rs7129220
AMPD3 ; CAND1.11
5 11 10328991 intron variant G/A snv 0.10 0.700 1.000 2 2011 2017
dbSNP: rs4373814
rs4373814 		5 10 18131043 intergenic variant G/C;T snv 0.700 1.000 1 2011 2011
dbSNP: rs6825911
rs6825911
ENPEP
3 4 110460482 intron variant C/T snv 0.68 0.700 1.000 1 2011 2011
dbSNP: rs805303
rs805303
BAG6
7 0.925 0.160 6 31648589 intron variant G/A snv 0.45 0.700 1.000 1 2011 2011
dbSNP: rs17080102
rs17080102
PLEKHG1
3 6 150683634 5 prime UTR variant G/C snv 8.6E-02 0.700 1.000 6 2013 2019
dbSNP: rs13209747
rs13209747 		5 6 126794309 intron variant C/G;T snv 0.36 0.700 1.000 4 2013 2018
dbSNP: rs17428471
rs17428471 		3 7 27298248 intergenic variant G/T snv 9.4E-02 0.700 1.000 2 2013 2017
dbSNP: rs10826334
rs10826334 		3 10 59620724 intron variant C/A;G snv 0.700 1.000 1 2013 2013
dbSNP: rs10832417
rs10832417
KCNQ1 ; KCNQ1OT1
3 11 2631427 non coding transcript exon variant T/G snv 0.32 0.700 1.000 1 2013 2013
dbSNP: rs10841530
rs10841530
PDE3A
2 12 20446178 intron variant A/G snv 0.30 0.700 1.000 1 2013 2013
dbSNP: rs11693319
rs11693319
CCDC141
2 2 178873542 3 prime UTR variant C/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs13178964
rs13178964 		2 5 105011948 intron variant A/G snv 0.17 0.700 1.000 1 2013 2013
dbSNP: rs1401454
rs1401454
SOX6
3 11 16228637 intron variant C/A;G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs1669539
rs1669539 		2 1.000 0.080 2 105998818 intergenic variant T/C snv 7.1E-02 0.700 1.000 1 2013 2013
dbSNP: rs16890334
rs16890334 		3 6 78846449 intergenic variant T/C snv 1.9E-03 0.700 1.000 1 2013 2013
dbSNP: rs16963349
rs16963349
WFDC1
2 16 84304628 intron variant T/C snv 7.4E-02 0.700 1.000 1 2013 2013
dbSNP: rs2410182
rs2410182 		2 21 39808149 intergenic variant A/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs2735413
rs2735413 		2 16 78019746 intron variant A/C;T snv 0.700 1.000 1 2013 2013