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: rs28933091
rs28933091
4 0.882 0.160 1 156134474 missense variant C/A;G snv 0.710 1.000 0 2001 2001
dbSNP: rs58034145
rs58034145
1 0.827 0.160 1 156134830 missense variant A/C snv 0.710 1.000 0 2005 2005
dbSNP: rs59653062
rs59653062
1 0.925 0.120 1 156136076 missense variant T/A snv 0.710 1.000 0 2006 2006
dbSNP: rs61672878
rs61672878
3 0.776 0.200 1 156136094 missense variant G/A;T snv 0.710 1.000 0 2004 2004
dbSNP: rs11575937
rs11575937
14 0.653 0.480 1 156136985 missense variant G/A;T snv 0.700 0
dbSNP: rs13768
rs13768
1 1.000 0.120 1 156138660 missense variant G/A;T snv 2.4E-05 0.700 0
dbSNP: rs142000963
rs142000963
3 0.807 0.240 1 156138719 missense variant C/A;T snv 1.2E-03 0.700 0
dbSNP: rs1553265999
rs1553265999
1 1.000 0.120 1 156136925 missense variant A/C snv 0.700 0
dbSNP: rs267607539
rs267607539
1 1.000 0.120 1 156137237 splice region variant G/A;C snv 0.700 0
dbSNP: rs267607540
rs267607540
1 1.000 0.120 1 156134509 inframe deletion GAA/- delins 0.700 0
dbSNP: rs267607632
rs267607632
4 0.851 0.120 1 156134976 splice donor variant G/A;C snv 0.700 0
dbSNP: rs28928901
rs28928901
3 0.882 0.120 1 156134829 missense variant C/T snv 0.700 0
dbSNP: rs386134243
rs386134243
16 0.708 0.360 1 156135967 missense variant C/A;T snv 4.0E-06 0.700 0
dbSNP: rs56694480
rs56694480
1 1.000 0.120 1 156115021 missense variant C/G snv 0.700 0
dbSNP: rs56699480
rs56699480
1 1.000 0.120 1 156137017 stop gained C/T snv 0.700 0
dbSNP: rs56771886
rs56771886
2 0.925 0.160 1 156135923 frameshift variant T/- delins 0.700 0
dbSNP: rs57747780
rs57747780
1 0.925 0.200 1 156136981 missense variant T/C snv 0.700 0
dbSNP: rs58048078
rs58048078
1 0.925 0.120 1 156134942 stop gained T/A;C snv 4.0E-06 0.700 0
dbSNP: rs58105277
rs58105277
1 1.000 0.120 1 156135971 missense variant G/A snv 2.8E-05 0.700 0
dbSNP: rs58327533
rs58327533
1 1.000 0.120 1 156114991 missense variant C/G;T snv 0.700 0
dbSNP: rs58362413
rs58362413
2 0.925 0.160 1 156137183 stop gained G/A;C snv 0.700 0
dbSNP: rs58436778
rs58436778
2 0.925 0.120 1 156115052 missense variant A/G snv 0.700 0
dbSNP: rs58541611
rs58541611
1 1.000 0.120 1 156136393 missense variant A/G;T snv 0.700 0
dbSNP: rs59931416
rs59931416
1 1.000 0.120 1 156115066 missense variant C/A;T snv 0.700 0
dbSNP: rs60446065
rs60446065
1 1.000 0.120 1 156115045 missense variant G/A snv 0.700 0