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: rs1553245943
rs1553245943
2 1.000 0.080 1 160137001 missense variant G/A snv 0.700 1.000 4 2008 2017
dbSNP: rs28933400
rs28933400
3 0.882 0.080 1 160135510 missense variant T/C snv 0.020 1.000 2 2003 2004
dbSNP: rs121918613
rs121918613
2 0.925 0.080 1 160128667 missense variant A/G snv 0.010 1.000 1 2004 2004
dbSNP: rs121918616
rs121918616
3 0.882 0.080 1 160130283 missense variant G/A snv 4.0E-06 0.010 1.000 1 2005 2005
dbSNP: rs28933401
rs28933401
3 0.882 0.120 1 160135246 missense variant G/A snv 0.010 1.000 1 2003 2003
dbSNP: rs746795369
rs746795369
6 0.827 0.080 1 160139969 missense variant C/A;T snv 1.2E-05; 4.0E-06 0.010 1.000 1 2013 2013
dbSNP: rs121908212
rs121908212
14 0.732 0.160 19 13303877 missense variant G/A snv 0.830 1.000 13 1996 2018
dbSNP: rs121908213
rs121908213
1 1.000 0.080 19 13303580 missense variant A/G snv 0.820 1.000 12 1996 2017
dbSNP: rs121908214
rs121908214
4 0.925 0.080 19 13230185 missense variant T/G snv 0.820 1.000 12 1996 2017
dbSNP: rs121908211
rs121908211
5 0.882 0.080 19 13371744 missense variant C/T snv 0.810 1.000 11 1996 2017
dbSNP: rs121908225
rs121908225
12 0.790 0.120 19 13365448 missense variant G/A snv 0.820 1.000 11 1996 2017
dbSNP: rs121908217
rs121908217
9 0.851 0.120 19 13308452 missense variant C/T snv 4.0E-06 0.800 1.000 10 1996 2017
dbSNP: rs121908218
rs121908218
2 0.925 0.080 19 13303576 missense variant G/A;C;T snv 0.800 1.000 10 1996 2017
dbSNP: rs121908219
rs121908219
1 1.000 0.080 19 13261552 missense variant T/C snv 0.800 1.000 10 1996 2017
dbSNP: rs121908220
rs121908220
2 0.925 0.120 19 13235685 missense variant G/A snv 0.800 1.000 10 1996 2017
dbSNP: rs121908221
rs121908221
1 1.000 0.080 19 13235637 missense variant A/G snv 0.700 1.000 10 1996 2017
dbSNP: rs121908222
rs121908222
1 1.000 0.080 19 13371735 missense variant C/T snv 0.700 1.000 10 1996 2017
dbSNP: rs121908223
rs121908223
2 0.925 0.080 19 13262823 missense variant T/C snv 0.700 1.000 10 1996 2017
dbSNP: rs121908224
rs121908224
2 1.000 0.080 19 13235262 missense variant C/T snv 0.700 1.000 10 1996 2017
dbSNP: rs121908230
rs121908230
5 0.882 0.080 19 13262789 missense variant C/T snv 0.800 1.000 10 1996 2017
dbSNP: rs121908237
rs121908237
1 1.000 0.080 19 13259589 missense variant C/A snv 0.800 1.000 10 1996 2017
dbSNP: rs1026872132
rs1026872132
1 1.000 0.080 19 13234934 missense variant T/C snv 7.0E-06 0.010 1.000 1 2016 2016
dbSNP: rs1402027664
rs1402027664
2 0.925 0.080 19 13312697 missense variant T/C snv 0.010 1.000 1 2005 2005
dbSNP: rs41276886
rs41276886
2 0.925 0.080 19 13317310 missense variant C/T snv 4.5E-03 4.4E-03 0.010 1.000 1 2010 2010
dbSNP: rs759252101
rs759252101
1 1.000 0.080 19 13212143 missense variant C/G snv 4.0E-06 0.010 < 0.001 1 2012 2012