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: rs12764182
rs12764182
LRMDA
1 10 76131488 intron variant T/G snv 0.16 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: 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: rs7562790
rs7562790
CRIM1
2 2 36446412 intron variant T/G snv 0.48 0.700 1.000 1 2016 2016
dbSNP: rs9436640
rs9436640
NFIA
2 1 61408005 intron variant T/G snv 0.44 0.700 1.000 1 2016 2016
dbSNP: rs11153730
rs11153730 		4 6 118346359 intergenic variant T/C snv 0.40 0.700 1.000 1 2016 2016
dbSNP: rs11700980
rs11700980
N6AMT1
1 21 28781917 regulatory region variant T/C snv 8.7E-02 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: 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: rs1991601
rs1991601
WIPF1
1 2 174603041 intron variant T/C snv 0.79 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: 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: rs7132327
rs7132327 		1 12 114943266 intergenic variant T/C snv 0.27 0.700 1.000 1 2016 2016
dbSNP: rs7771320
rs7771320 		1 6 7502516 upstream gene variant T/C snv 5.4E-02 0.700 1.000 1 2016 2016
dbSNP: rs7909027
rs7909027
CACNB2
1 10 18406963 intron variant T/C snv 0.44 0.700 1.000 1 2016 2016
dbSNP: rs7198919
rs7198919
LITAF
1 16 11595035 intron variant T/A;C snv 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: rs12880291
rs12880291
SIPA1L1
1 14 71417850 intron variant G/T snv 0.18 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: rs7342028
rs7342028
VTI1A
2 10 112719503 intron variant G/C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs11708996
rs11708996
SCN5A
6 0.925 0.120 3 38592432 intron variant G/C snv 0.11 0.700 1.000 1 2016 2016
dbSNP: rs879568
rs879568
FHOD3
1 18 36731696 intron variant G/C snv 0.40 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: rs9470361
rs9470361 		12 0.776 0.080 6 36655602 regulatory region variant G/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs1344852
rs1344852 		1 4 20182314 intergenic variant G/A;C;T snv 0.700 1.000 1 2016 2016