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: rs1187878
rs1187878
1 14 55026632 intron variant T/C snv 0.59 0.700 1.000 1 2012 2012
dbSNP: rs1201378
rs1201378
1 14 55026690 intron variant T/A;C snv 0.57 0.700 1.000 1 2012 2012
dbSNP: rs1209087
rs1209087
1 14 55026502 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10139354
rs10139354
1 14 55011884 intron variant C/T snv 0.43 0.700 1.000 1 2012 2012
dbSNP: rs10140164
rs10140164
1 14 54939405 3 prime UTR variant A/G snv 0.50 0.700 1.000 1 2012 2012
dbSNP: rs11627963
rs11627963
1 14 54959829 intron variant C/G snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs1187882
rs1187882
1 14 55022029 intron variant C/G snv 0.62 0.700 1.000 1 2012 2012
dbSNP: rs1187883
rs1187883
1 14 55021516 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs17128120
rs17128120
1 14 55007880 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs17253633
rs17253633
1 14 55003199 intron variant T/C snv 0.17 0.700 1.000 1 2012 2012
dbSNP: rs17832269
rs17832269
1 14 54965373 intron variant C/T snv 0.29 0.700 1.000 1 2012 2012
dbSNP: rs2878174
rs2878174
1 14 55003906 intron variant T/C snv 0.51 0.700 1.000 1 2012 2012
dbSNP: rs4335711
rs4335711
1 14 55004145 intron variant G/C snv 0.28 0.700 1.000 1 2012 2012
dbSNP: rs7146285
rs7146285
1 14 54946151 intron variant T/C snv 0.43 0.700 1.000 1 2012 2012
dbSNP: rs7151670
rs7151670
1 14 54986041 intron variant C/G snv 0.30 0.700 1.000 1 2012 2012
dbSNP: rs7153937
rs7153937
1 14 55004157 intron variant A/G snv 0.43 0.700 1.000 1 2012 2012
dbSNP: rs8009997
rs8009997
1 14 54955193 intron variant T/G snv 0.29 0.700 1.000 1 2012 2012
dbSNP: rs8012152
rs8012152
1 14 54958849 intron variant T/C snv 0.43 0.700 1.000 1 2012 2012
dbSNP: rs8018800
rs8018800
1 14 54986588 intron variant A/G snv 0.43 0.700 1.000 1 2012 2012
dbSNP: rs8019220
rs8019220
1 14 54986751 intron variant C/T snv 0.43 0.700 1.000 1 2012 2012
dbSNP: rs8019390
rs8019390
1 14 54942366 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs8020545
rs8020545
1 14 54942352 intron variant T/A snv 0.35 0.700 1.000 1 2012 2012
dbSNP: rs8022049
rs8022049
1 14 54996151 intron variant T/C snv 0.30 0.700 1.000 1 2012 2012
dbSNP: rs9285583
rs9285583
1 14 54964717 intron variant T/C snv 0.43 0.700 1.000 1 2012 2012
dbSNP: rs943914
rs943914
1 14 54973350 intron variant C/A snv 0.34 0.700 1.000 1 2012 2012