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: rs12548036
rs12548036
1 1.000 0.080 8 128935636 intron variant G/A;T snv 0.700 1.000 2 2010 2012
dbSNP: rs1519841
rs1519841
1 1.000 0.080 8 128907554 intron variant T/C;G snv 0.700 1.000 2 2010 2012
dbSNP: rs2395855
rs2395855
1 1.000 0.080 8 128828493 intron variant T/A;C snv 0.700 1.000 2 2010 2012
dbSNP: rs4733532
rs4733532
1 1.000 0.080 8 128869053 intron variant G/A;C snv 0.700 1.000 2 2010 2012
dbSNP: rs1030609
rs1030609
1 1.000 0.080 8 128727631 intron variant C/A;G snv 0.700 1.000 1 2012 2012
dbSNP: rs2197111
rs2197111
1 1.000 0.080 8 129003469 intron variant A/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs3857888
rs3857888
1 1.000 0.080 8 128812615 intron variant G/C;T snv 0.700 1.000 1 2009 2009
dbSNP: rs7006281
rs7006281
1 1.000 0.080 8 128788524 intron variant A/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs748978
rs748978
1 1.000 0.080 8 128990870 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs7835741
rs7835741
1 1.000 0.080 8 129005468 intron variant T/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs7838330
rs7838330
1 1.000 0.080 8 128980860 intron variant T/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs997310
rs997310
1 1.000 0.080 8 128908034 intron variant C/A;G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs17820135
rs17820135
1 1.000 0.080 8 128935540 intron variant T/G snv 6.0E-02 0.700 1.000 1 2009 2009
dbSNP: rs17821251
rs17821251
1 1.000 0.080 8 128996987 intron variant T/C snv 6.3E-02 0.700 1.000 1 2009 2009
dbSNP: rs12546244
rs12546244
1 1.000 0.080 8 128958000 intron variant G/A snv 0.11 0.700 1.000 1 2009 2009
dbSNP: rs4422741
rs4422741
1 1.000 0.080 8 129199082 intron variant T/C snv 0.11 0.700 1.000 1 2012 2012
dbSNP: rs3935421
rs3935421
1 1.000 0.080 8 129190893 intron variant A/G snv 0.13 0.700 1.000 1 2012 2012
dbSNP: rs17241253
rs17241253
1 1.000 0.080 8 128877942 intron variant T/C snv 0.13 0.700 1.000 1 2009 2009
dbSNP: rs72728734
rs72728734
3 0.882 0.120 8 128921474 intron variant A/G snv 0.13 0.700 1.000 1 2017 2017
dbSNP: rs7826130
rs7826130
1 1.000 0.080 8 129212496 intron variant C/T snv 0.13 0.700 1.000 1 2009 2009
dbSNP: rs7822386
rs7822386
1 1.000 0.080 8 129212475 intron variant A/G snv 0.13 0.700 1.000 1 2012 2012
dbSNP: rs7826294
rs7826294
1 1.000 0.080 8 129212646 intron variant C/T snv 0.13 0.700 1.000 1 2009 2009
dbSNP: rs7826688
rs7826688
1 1.000 0.080 8 129212765 intron variant G/A snv 0.13 0.700 1.000 1 2012 2012
dbSNP: rs4472475
rs4472475
1 1.000 0.080 8 129209789 intron variant A/G snv 0.13 0.700 1.000 1 2009 2009
dbSNP: rs55658222
rs55658222
2 0.925 0.120 8 128963890 intron variant G/A snv 0.14 0.700 1.000 1 2017 2017