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: rs10507391
rs10507391
10 0.776 0.320 13 30737959 intron variant A/T snv 0.52 0.040 1.000 4 2011 2016
dbSNP: rs9551963
rs9551963
6 0.851 0.160 13 30758410 intron variant A/C;T snv 0.020 1.000 2 2014 2015
dbSNP: rs12429692
rs12429692
2 1.000 0.080 13 30738041 intron variant A/T snv 0.24 0.010 1.000 1 2011 2011
dbSNP: rs17222919
rs17222919
2 1.000 0.080 13 30734192 intron variant T/A;G snv 0.010 1.000 1 2018 2018
dbSNP: rs3803277
rs3803277
1 13 30744171 non coding transcript exon variant C/A snv 0.49 0.45 0.010 1.000 1 2014 2014
dbSNP: rs4769060
rs4769060
1 13 30763740 intron variant A/G snv 0.35 0.010 1.000 1 2015 2015
dbSNP: rs9579646
rs9579646
6 0.851 0.160 13 30736442 intron variant G/A;T snv 0.010 1.000 1 2011 2011