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: rs10176820
rs10176820
IL18RAP
1 2 102437960 intron variant T/C snv 0.24 0.700 1.000 1 2013 2013
dbSNP: rs10177758
rs10177758
PLCL1
1 2 197994193 intron variant A/G snv 0.48 0.700 1.000 1 2013 2013
dbSNP: rs10178214
rs10178214
IL1RL2
1 2 102242461 downstream gene variant G/T snv 0.24 0.700 1.000 1 2013 2013
dbSNP: rs10181785
rs10181785 		1 2 102408814 upstream gene variant C/T snv 0.22 0.700 1.000 1 2013 2013
dbSNP: rs10184227
rs10184227
PLCL1
1 2 198029581 intron variant C/T snv 0.48 0.700 1.000 1 2013 2013
dbSNP: rs10184395
rs10184395
PLCL1
1 2 198029561 intron variant G/A snv 0.69 0.700 1.000 1 2013 2013
dbSNP: rs10189897
rs10189897
PLCL1
1 2 197948686 intron variant A/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs10190226
rs10190226
PLCL1
1 2 198036840 intron variant C/T snv 0.69 0.700 1.000 1 2013 2013
dbSNP: rs10192466
rs10192466
PLCL1
1 2 197873295 intron variant G/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs10196612
rs10196612
PLCL1
1 2 198029415 intron variant T/C snv 0.49 0.700 1.000 1 2013 2013
dbSNP: rs10196961
rs10196961
RFTN2
1 2 197649206 intron variant G/A snv 0.47 0.700 1.000 1 2013 2013
dbSNP: rs10197310
rs10197310 		1 2 102403570 downstream gene variant T/A snv 0.22 0.700 1.000 1 2013 2013
dbSNP: rs10198606
rs10198606
PLCL1
1 2 197905015 intron variant C/A;G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs10202813
rs10202813 		1 2 102403280 downstream gene variant G/T snv 0.22 0.700 1.000 1 2013 2013
dbSNP: rs10206714
rs10206714
PLCL1
1 2 198041757 intron variant C/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs10207433
rs10207433
PLCL1
1 2 197941206 intron variant G/T snv 0.51 0.700 1.000 1 2013 2013
dbSNP: rs10210006
rs10210006
LINC00299
1 2 8326356 intron variant C/G snv 0.29 0.700 1.000 1 2013 2013
dbSNP: rs10210176
rs10210176 		1 2 102463056 intergenic variant C/A snv 0.22 0.700 1.000 1 2013 2013
dbSNP: rs1022804
rs1022804
TTC6
1 14 37711608 intron variant G/A snv 0.20 0.700 1.000 1 2013 2013
dbSNP: rs1031163
rs1031163 		1 10 9015459 regulatory region variant G/T snv 0.33 0.700 1.000 1 2013 2013
dbSNP: rs1035765
rs1035765
LPP
1 3 188402995 intron variant A/T snv 0.38 0.700 1.000 1 2013 2013
dbSNP: rs1035766
rs1035766
LPP
1 3 188402952 intron variant G/A snv 0.38 0.700 1.000 1 2013 2013
dbSNP: rs1036333
rs1036333
PLCL1
1 2 198079063 intron variant G/T snv 0.51 0.700 1.000 1 2013 2013
dbSNP: rs1044265
rs1044265
EMSY
1 11 76551084 3 prime UTR variant A/G snv 0.40 0.700 1.000 1 2013 2013
dbSNP: rs10447257
rs10447257 		1 5 110845538 intergenic variant T/C;G snv 0.700 1.000 1 2013 2013