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: rs13192235
rs13192235
2 6 135025213 intron variant G/A snv 4.0E-02 0.700 1.000 1 2012 2012
dbSNP: rs13196486
rs13196486
1 6 134962736 3 prime UTR variant C/G snv 0.31 0.700 1.000 1 2012 2012
dbSNP: rs13197750
rs13197750
1 6 134991242 intron variant G/A snv 0.31 0.700 1.000 1 2012 2012
dbSNP: rs13199205
rs13199205
1 6 134965367 intron variant T/A;C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs13209780
rs13209780
1 6 135023657 intron variant G/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs13214669
rs13214669
1 6 134978821 intron variant T/C snv 0.33 0.31 0.700 1.000 1 2012 2012
dbSNP: rs13218642
rs13218642
1 6 134988802 intron variant A/G snv 0.46 0.700 1.000 1 2012 2012
dbSNP: rs13220662
rs13220662
4 6 135074410 intron variant G/A snv 0.41 0.700 1.000 1 2012 2012
dbSNP: rs1331308
rs1331308
2 6 135083984 intron variant A/C snv 0.61 0.700 1.000 1 2012 2012
dbSNP: rs1547247
rs1547247
5 6 135069698 intron variant G/A snv 0.22 0.700 1.000 1 2012 2012
dbSNP: rs1590975
rs1590975
1 6 135030950 intron variant C/T snv 0.53 0.700 1.000 1 2012 2012
dbSNP: rs2150681
rs2150681
1 6 135054094 intron variant C/T snv 0.50 0.700 1.000 1 2012 2012
dbSNP: rs2183709
rs2183709
1 6 135055953 intron variant C/T snv 0.46 0.700 1.000 1 2012 2012
dbSNP: rs2210366
rs2210366
4 6 135094070 intron variant G/A snv 0.34 0.700 1.000 1 2012 2012
dbSNP: rs2297338
rs2297338
1 6 135054624 intron variant G/A snv 0.51 0.46 0.700 1.000 1 2012 2012
dbSNP: rs2327578
rs2327578
1 6 135008831 intron variant C/T snv 0.46 0.700 1.000 1 2012 2012
dbSNP: rs3756799
rs3756799
1 6 135019873 intron variant A/G snv 0.46 0.700 1.000 1 2012 2012
dbSNP: rs4142299
rs4142299
1 6 135056048 intron variant G/T snv 0.46 0.700 1.000 1 2012 2012
dbSNP: rs4451151
rs4451151
1 6 134989408 intron variant C/T snv 0.46 0.700 1.000 1 2012 2012
dbSNP: rs4594969
rs4594969
1 6 134964448 3 prime UTR variant A/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs4895434
rs4895434
1 6 134972227 intron variant G/A snv 0.62 0.700 1.000 1 2012 2012
dbSNP: rs4895435
rs4895435
1 6 134972325 intron variant C/A snv 0.62 0.700 1.000 1 2012 2012
dbSNP: rs4895436
rs4895436
1 6 134973863 intron variant G/A snv 0.46 0.700 1.000 1 2012 2012
dbSNP: rs4895438
rs4895438
1 6 134996527 intron variant G/T snv 0.49 0.700 1.000 1 2012 2012
dbSNP: rs4895439
rs4895439
1 6 134997716 intron variant A/G;T snv 0.700 1.000 1 2012 2012