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: rs104893807
rs104893807
2 0.925 0.120 3 30674196 missense variant C/G;T snv 0.800 1.000 13 2004 2017
dbSNP: rs104893809
rs104893809
3 0.882 0.120 3 30691504 missense variant C/T snv 0.800 1.000 13 2004 2017
dbSNP: rs104893810
rs104893810
7 0.790 0.360 3 30691477 missense variant C/T snv 0.800 1.000 13 2004 2017
dbSNP: rs104893811
rs104893811
4 0.851 0.160 3 30674228 missense variant C/T snv 0.800 1.000 13 2004 2017
dbSNP: rs104893812
rs104893812
1 1.000 0.120 3 30672189 missense variant T/A;G snv 0.800 1.000 13 2004 2017
dbSNP: rs104893813
rs104893813
1 1.000 0.120 3 30672246 missense variant G/A;C;T snv 8.2E-06; 8.2E-06 0.800 1.000 13 2004 2017
dbSNP: rs104893814
rs104893814
1 1.000 0.120 3 30672252 missense variant G/T snv 0.800 1.000 13 2004 2017
dbSNP: rs104893815
rs104893815
4 0.851 0.240 3 30691478 missense variant G/A snv 0.800 1.000 13 2004 2017
dbSNP: rs104893816
rs104893816
3 0.882 0.120 3 30674229 missense variant G/A;T snv 4.0E-06 0.800 1.000 13 2004 2017
dbSNP: rs28934568
rs28934568
1 1.000 0.120 3 30672106 missense variant T/C snv 0.800 1.000 13 2004 2017
dbSNP: rs1553630274
rs1553630274
1 1.000 0.120 3 30672313 missense variant A/G snv 0.700 1.000 10 2004 2012
dbSNP: rs761231369
rs761231369
1 1.000 0.120 3 30671923 missense variant A/T snv 8.0E-06 1.4E-05 0.700 1.000 10 2004 2012
dbSNP: rs780542125
rs780542125
1 1.000 0.120 3 30671752 missense variant G/A snv 5.2E-05 2.8E-05 0.700 1.000 3 2013 2017
dbSNP: rs1553630457
rs1553630457
8 0.882 0.240 3 30674231 missense variant T/C snv 0.700 1.000 1 2017 2017
dbSNP: rs104893817
rs104893817
1 1.000 0.120 3 30674123 missense variant A/C;G snv 0.700 0
dbSNP: rs104893818
rs104893818
1 1.000 0.120 3 30674130 missense variant C/T snv 0.700 0
dbSNP: rs104893819
rs104893819
5 0.827 0.240 3 30688470 stop gained C/G;T snv 0.700 0
dbSNP: rs121918715
rs121918715
1 1.000 0.120 3 30688511 splice region variant G/A snv 0.700 0
dbSNP: rs193922664
rs193922664
2 0.925 0.120 3 30691435 missense variant T/C snv 0.700 0
dbSNP: rs587776770
rs587776770
1 1.000 0.120 3 30688382 splice acceptor variant A/G snv 0.700 0
dbSNP: rs727504292
rs727504292
3 0.882 0.120 3 30672250 missense variant G/A;C snv 1.6E-05 0.700 0
dbSNP: rs727504421
rs727504421
3 0.882 0.160 3 30691465 missense variant G/A;T snv 0.700 0
dbSNP: rs863223852
rs863223852
4 0.882 0.120 3 30688476 stop gained C/A;T snv 4.0E-06 0.700 0
dbSNP: rs863223853
rs863223853
1 1.000 0.120 3 30691421 missense variant G/T snv 0.700 0
dbSNP: rs863224935
rs863224935
1 1.000 0.120 3 30688395 missense variant T/G snv 0.700 0