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: rs35887622
rs35887622
8 0.790 0.200 13 20189481 missense variant A/C;G snv 8.7E-03 0.040 1.000 4 1998 2019
dbSNP: rs104894396
rs104894396
28 0.672 0.400 13 20189511 stop gained C/T snv 5.8E-04 1.1E-04 0.020 1.000 2 2010 2011
dbSNP: rs28931593
rs28931593
9 0.776 0.200 13 20189358 missense variant C/T snv 7.0E-06 0.020 1.000 2 2005 2015
dbSNP: rs72474224
rs72474224
18 0.708 0.440 13 20189473 missense variant C/A;T snv 7.7E-03 0.020 1.000 2 2015 2019
dbSNP: rs1064797088
rs1064797088
2 0.925 0.120 13 20189446 missense variant C/T snv 0.010 1.000 1 2011 2011
dbSNP: rs111033293
rs111033293
10 0.763 0.280 13 20189581 start lost T/A;C snv 3.6E-05 4.2E-05 0.010 1.000 1 2009 2009
dbSNP: rs117685390
rs117685390
1 1.000 0.120 13 20193170 upstream gene variant A/G snv 0.16 0.010 1.000 1 2013 2013
dbSNP: rs2274083
rs2274083
3 0.925 0.200 13 20189241 missense variant T/C snv 1.5E-02 5.1E-03 0.010 1.000 1 2016 2016
dbSNP: rs2274084
rs2274084
6 0.882 0.240 13 20189503 missense variant C/T snv 5.4E-02 2.2E-02 0.010 1.000 1 2016 2016