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: rs6313
rs6313
82 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 0.010 < 0.001 1 2001 2001
dbSNP: rs5770917
rs5770917
2 0.925 0.080 22 50578924 intron variant T/C snv 6.0E-02 0.840 0.750 4 2008 2014
dbSNP: rs1154155
rs1154155
2 0.925 0.080 14 22533736 upstream gene variant G/A;T snv 0.810 1.000 5 2009 2015
dbSNP: rs10995245
rs10995245
3 0.882 0.160 10 62631615 intron variant G/A;C snv 0.800 1.000 2 2013 2013
dbSNP: rs10013443
rs10013443
1 1.000 0.080 4 168685769 intron variant T/C snv 3.4E-02 0.700 1.000 1 2009 2009
dbSNP: rs10024442
rs10024442
1 1.000 0.080 4 153570903 intron variant T/G snv 0.13 0.700 1.000 1 2009 2009
dbSNP: rs10032741
rs10032741
1 1.000 0.080 4 44958427 intergenic variant T/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs10035360
rs10035360
1 1.000 0.080 5 34604531 regulatory region variant C/T snv 0.19 0.700 1.000 1 2009 2009
dbSNP: rs10045595
rs10045595
1 1.000 0.080 5 167802999 intron variant T/G snv 0.36 0.700 1.000 1 2009 2009
dbSNP: rs10049436
rs10049436
2 1.000 0.080 3 165771478 intron variant C/T snv 8.1E-02 0.700 1.000 1 2009 2009
dbSNP: rs10091183
rs10091183
1 1.000 0.080 8 33215980 regulatory region variant A/G snv 4.6E-02 0.700 1.000 1 2009 2009
dbSNP: rs10094069
rs10094069
1 1.000 0.080 8 113022302 intron variant C/T snv 0.59 0.700 1.000 1 2009 2009
dbSNP: rs1009449
rs1009449
1 1.000 0.080 11 33684620 intron variant A/G snv 4.2E-03 0.700 1.000 1 2009 2009
dbSNP: rs1011356
rs1011356
1 1.000 0.080 14 76678871 intron variant C/A;G snv 0.700 1.000 1 2009 2009
dbSNP: rs10160659
rs10160659
1 1.000 0.080 11 6644463 intron variant A/C snv 5.5E-02 0.700 1.000 1 2009 2009
dbSNP: rs10200800
rs10200800
1 1.000 0.080 2 223088118 intron variant T/C snv 0.75 0.700 1.000 1 2009 2009
dbSNP: rs10226621
rs10226621
1 1.000 0.080 7 4068008 intron variant A/C;G snv 0.700 1.000 1 2009 2009
dbSNP: rs10240026
rs10240026
1 1.000 0.080 7 142491501 upstream gene variant A/T snv 6.8E-02 0.700 1.000 1 2009 2009
dbSNP: rs10418441
rs10418441
1 1.000 0.080 19 17569292 intron variant C/A;T snv 0.700 1.000 1 2009 2009
dbSNP: rs10484565
rs10484565
2 0.925 0.200 6 32827255 3 prime UTR variant G/A snv 6.1E-02 0.700 1.000 1 2009 2009
dbSNP: rs10487465
rs10487465
1 1.000 0.080 7 127056727 intron variant T/C snv 7.9E-02 0.700 1.000 1 2009 2009
dbSNP: rs10490165
rs10490165
1 1.000 0.080 2 50961428 intron variant T/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs10775354
rs10775354
1 1.000 0.080 16 6757689 intron variant A/C;T snv 0.700 1.000 1 2009 2009
dbSNP: rs10780661
rs10780661
1 1.000 0.080 9 84311392 intron variant A/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs1086603
rs1086603
3 0.882 0.120 1 147816164 intergenic variant G/A snv 3.4E-02 0.700 1.000 1 2009 2009