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: rs1022491
rs1022491
1 6 134938228 intron variant C/T snv 0.60 0.700 1.000 1 2012 2012
dbSNP: rs2064101
rs2064101
1 6 134929392 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs2072825
rs2072825
1 6 134932313 intron variant A/G snv 0.67 0.700 1.000 1 2012 2012
dbSNP: rs2072826
rs2072826
1 6 134932420 intron variant G/C snv 0.67 0.700 1.000 1 2012 2012
dbSNP: rs2072827
rs2072827
1 6 134932465 intron variant G/A snv 0.34 0.700 1.000 1 2012 2012
dbSNP: rs2142725
rs2142725
1 6 134937804 intron variant T/G snv 0.63 0.700 1.000 1 2012 2012
dbSNP: rs2294321
rs2294321
1 6 134931910 intron variant T/G snv 0.67 0.700 1.000 1 2012 2012
dbSNP: rs3817776
rs3817776
1 6 134935618 intron variant C/T snv 0.50 0.700 1.000 1 2012 2012
dbSNP: rs4267967
rs4267967
1 6 134951339 upstream gene variant T/G snv 0.47 0.700 1.000 1 2012 2012
dbSNP: rs4646868
rs4646868
1 6 134950808 upstream gene variant A/G snv 0.45 0.700 1.000 1 2012 2012
dbSNP: rs4646870
rs4646870
1 6 134950190 upstream gene variant C/A snv 0.32 0.700 1.000 1 2012 2012
dbSNP: rs4646871
rs4646871
1 6 134944479 intron variant G/A snv 0.49 0.700 1.000 1 2012 2012
dbSNP: rs728030
rs728030
1 6 134925156 intron variant C/A snv 0.65 0.700 1.000 1 2012 2012
dbSNP: rs7754722
rs7754722
1 6 134939165 intron variant T/C snv 0.68 0.700 1.000 1 2012 2012
dbSNP: rs7771310
rs7771310
1 6 134951397 upstream gene variant G/A snv 0.34 0.700 1.000 1 2012 2012
dbSNP: rs7772031
rs7772031
1 6 134938596 intron variant G/A;T snv 0.700 1.000 1 2012 2012