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: rs121909237
rs121909237
1 1.000 0.036 10 87933121 stop gained C/G snp 0.800 1 2002 2002
dbSNP: rs121912666
rs121912666
29 0.647 0.321 17 7674872 missense variant T/C,G snp 8.0E-06 0.710 1.000 2 2007 2016
dbSNP: rs121913433
rs121913433
1 1.000 0.036 7 55174771 missense variant A/G snp 0.700 3 2010 2015
dbSNP: rs1023835002
rs1023835002
10 0.756 0.250 15 44711547 start lost A/G snp 0.700 1 2016 2016
dbSNP: rs104886003
rs104886003
52 0.580 0.393 3 179218303 missense variant G/A,C snp 4.0E-06 0.700 1 2016 2016
dbSNP: rs104894104
rs104894104
7 0.784 0.143 9 21971019 missense variant G/A,T snp 0.700 1 2016 2016
dbSNP: rs104894226
rs104894226
19 0.692 0.464 11 534285 missense variant C/A,G,T snp 0.700 1 2016 2016
dbSNP: rs104894228
rs104894228
26 0.662 0.500 11 534286 missense variant C/A,G,T snp 0.700 1 2016 2016
dbSNP: rs104894229
rs104894229
31 0.634 0.500 11 534289 missense variant C/A,G,T snp 0.700 1 2016 2016
dbSNP: rs104894230
rs104894230
42 0.615 0.464 11 534288 missense variant C/A,G,T snp 0.700 1 2016 2016
dbSNP: rs1057519747
rs1057519747
17 0.715 0.250 17 7675094 missense variant A/C,G,T snp 0.700 1 2016 2016
dbSNP: rs1057519816
rs1057519816
9 0.801 0.214 17 39711955 missense variant C/A,T snp 0.700 1 2016 2016
dbSNP: rs1057519874
rs1057519874
5 0.821 0.107 7 6387261 missense variant C/A,T snp 0.700 1 2016 2016
dbSNP: rs1057519877
rs1057519877
10 0.756 0.250 15 44711549 start lost G/A snp 0.700 1 2016 2016
dbSNP: rs1057519879
rs1057519879
10 0.756 0.250 15 44711548 start lost T/C,G snp 0.700 1 2016 2016
dbSNP: rs1057519881
rs1057519881
8 0.769 0.250 9 21971111 missense variant T/C snp 0.700 1 2016 2016
dbSNP: rs1057519882
rs1057519882
7 0.801 0.179 9 21974678 missense variant C/A snp 0.700 1 2016 2016
dbSNP: rs1057519883
rs1057519883
11 0.744 0.250 9 21971120 missense variant C/G,T snp 3.2E-05 0.700 1 2016 2016
dbSNP: rs1057519884
rs1057519884
10 0.756 0.214 16 3738616 missense variant C/A,T snp 0.700 1 2016 2016
dbSNP: rs1057519887
rs1057519887
3 0.923 0.036 7 55154128 missense variant GC/AA,AT multinucleotide-polymorphism 0.700 1 2016 2016
dbSNP: rs1057519889
rs1057519889
5 0.821 0.179 22 41169525 missense variant G/A,T snp 0.700 1 2016 2016
dbSNP: rs1057519895
rs1057519895
13 0.734 0.214 4 152328232 missense variant C/A,G,T snp 0.700 1 2016 2016
dbSNP: rs1057519896
rs1057519896
11 0.744 0.286 4 152326136 missense variant C/A,T snp 0.700 1 2016 2016
dbSNP: rs1057519904
rs1057519904
2 0.923 0.071 6 27872233 missense variant T/A snp 0.700 1 2016 2016
dbSNP: rs1057519905
rs1057519905
2 0.923 0.071 6 27872234 missense variant T/C snp 0.700 1 2016 2016