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: rs9533090
rs9533090
3 13 42377313 intron variant C/T snv 0.39 0.800 1.000 4 2009 2018
dbSNP: rs9594738
rs9594738
1 13 42378009 intron variant C/T snv 0.39 0.800 1.000 3 2008 2018
dbSNP: rs9594759
rs9594759
1 13 42458457 intron variant C/T snv 0.51 0.800 1.000 3 2008 2009
dbSNP: rs7992970
rs7992970
1 13 42371327 intron variant A/G snv 0.26 0.700 1.000 2 2009 2009
dbSNP: rs8001611
rs8001611
2 13 42391558 intron variant C/T snv 0.59 0.700 1.000 2 2013 2018
dbSNP: rs9533095
rs9533095
2 13 42394913 intron variant G/T snv 0.39 0.700 1.000 2 2014 2018
dbSNP: rs10507508
rs10507508
1 13 42395646 intron variant A/G snv 6.2E-02 0.700 1.000 1 2009 2009
dbSNP: rs10507509
rs10507509
1 13 42398954 intron variant C/T snv 6.2E-02 0.700 1.000 1 2009 2009
dbSNP: rs11840862
rs11840862
1 13 42382327 intron variant A/G snv 0.56 0.700 1.000 1 2009 2009
dbSNP: rs11842146
rs11842146
1 13 42348370 intron variant C/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs12429224
rs12429224
1 13 42457917 intron variant G/T snv 0.40 0.700 1.000 1 2009 2009
dbSNP: rs12430303
rs12430303
1 13 42457891 intron variant T/C snv 0.43 0.700 1.000 1 2009 2009
dbSNP: rs12854504
rs12854504
1 13 42409565 intron variant T/G snv 6.2E-02 0.700 1.000 1 2009 2009
dbSNP: rs12873631
rs12873631
1 13 42394260 intron variant T/C snv 6.2E-02 0.700 1.000 1 2009 2009
dbSNP: rs12874234
rs12874234
1 13 42396587 intron variant A/G snv 6.2E-02 0.700 1.000 1 2009 2009
dbSNP: rs1324003
rs1324003
1 13 42401990 intron variant C/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs1475249
rs1475249
1 13 42380369 intron variant A/G snv 0.26 0.700 1.000 1 2009 2009
dbSNP: rs17063206
rs17063206
1 13 42343323 intron variant C/T snv 0.16 0.700 1.000 1 2009 2009
dbSNP: rs17457561
rs17457561
1 13 42390067 intron variant G/A snv 0.21 0.700 1.000 1 2009 2009
dbSNP: rs17638544
rs17638544
1 13 42382485 intron variant C/T snv 6.2E-02 0.700 1.000 1 2009 2009
dbSNP: rs180851
rs180851
1 13 42359904 intron variant C/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs1853573
rs1853573
1 13 42460832 intron variant G/C;T snv 0.46 0.700 1.000 1 2009 2009
dbSNP: rs2062305
rs2062305
2 1.000 0.040 13 42478744 intron variant G/A snv 0.46 0.700 1.000 1 2009 2009
dbSNP: rs238252
rs238252
1 13 42341518 intron variant C/G snv 0.17 0.700 1.000 1 2009 2009
dbSNP: rs238255
rs238255
1 13 42349225 intron variant G/A snv 0.42 0.700 1.000 1 2009 2009