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: rs114002140
rs114002140
1 1.000 0.040 6 32464185 intron variant A/G snv 0.700 1.000 1 2013 2013
dbSNP: rs114455101
rs114455101
2 1.000 0.040 6 32465853 intron variant T/G snv 0.700 1.000 1 2017 2017
dbSNP: rs115406947
rs115406947
1 1.000 0.040 6 32464869 intron variant G/A;C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs138984909
rs138984909
2 1.000 0.040 6 32466042 intron variant A/G snv 0.700 1.000 1 2017 2017
dbSNP: rs149998036
rs149998036
2 1.000 0.040 6 32470272 intron variant A/C;T snv 0.700 1.000 1 2017 2017
dbSNP: rs186229361
rs186229361
2 1.000 0.040 6 32468178 intron variant T/C snv 0.700 1.000 1 2017 2017
dbSNP: rs187696124
rs187696124
1 1.000 0.040 6 32469754 intron variant T/C snv 0.700 1.000 1 2015 2015
dbSNP: rs9268856
rs9268856
6 0.807 0.240 6 32461942 intron variant C/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs9268862
rs9268862
2 0.925 0.160 6 32462390 intron variant A/C snv 0.29 0.700 1.000 1 2013 2013
dbSNP: rs9268895
rs9268895
1 1.000 0.040 6 32464185 intron variant A/G snv 0.29 0.700 1.000 1 2013 2013