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: rs63749994
rs63749994
1 1.000 0.080 3 36993638 missense variant GC/TG mnv 0.700 1.000 20 1996 2012
dbSNP: rs63750012
rs63750012
1 1.000 0.080 3 37011827 missense variant G/A;C snv 4.0E-06 0.700 1.000 20 1996 2012
dbSNP: rs63750016
rs63750016
2 0.925 0.160 3 37047553 missense variant C/A;T snv 0.700 1.000 20 1996 2012
dbSNP: rs63750059
rs63750059
2 0.925 0.160 3 37042276 missense variant T/A;C;G snv 0.700 1.000 20 1996 2012
dbSNP: rs63750062
rs63750062
1 1.000 0.080 3 37042293 missense variant A/T snv 8.0E-06 0.700 1.000 20 1996 2012
dbSNP: rs63750144
rs63750144
3 0.925 0.160 3 37017599 missense variant G/A;C snv 0.700 1.000 20 1996 2012
dbSNP: rs63750193
rs63750193
6 0.851 0.160 3 37040276 missense variant T/C snv 0.700 1.000 20 1996 2012
dbSNP: rs63750211
rs63750211
5 0.882 0.160 3 37008904 missense variant A/G snv 0.700 1.000 20 1996 2012
dbSNP: rs63750240
rs63750240
1 1.000 0.080 3 37047679 missense variant A/C;G snv 0.700 1.000 20 1996 2012
dbSNP: rs63750271
rs63750271
1 1.000 0.080 3 37040279 missense variant A/C;G snv 8.0E-06 0.700 1.000 20 1996 2012
dbSNP: rs63750281
rs63750281
2 0.925 0.160 3 36996705 missense variant T/A snv 0.700 1.000 20 1996 2012
dbSNP: rs63750286
rs63750286
1 1.000 0.080 3 37020387 missense variant G/A;T snv 4.0E-06 0.700 1.000 20 1996 2012
dbSNP: rs63750289
rs63750289
1 1.000 0.080 3 37040273 missense variant T/C snv 0.700 1.000 20 1996 2012
dbSNP: rs63750303
rs63750303
4 0.882 0.160 3 37014485 missense variant G/A;T snv 0.700 1.000 20 1996 2012
dbSNP: rs63750314
rs63750314
1 1.000 0.080 3 37028827 missense variant G/C;T snv 0.700 1.000 20 1996 2012
dbSNP: rs63750453
rs63750453
5 0.882 0.160 3 37001051 missense variant G/A snv 0.700 1.000 20 1996 2012
dbSNP: rs63750507
rs63750507
2 0.925 0.160 3 37004414 missense variant T/G snv 4.0E-06 0.700 1.000 20 1996 2012
dbSNP: rs63750511
rs63750511
2 0.925 0.160 3 37040252 missense variant A/C;T snv 0.700 1.000 20 1996 2012
dbSNP: rs63750515
rs63750515
2 0.925 0.160 3 37011828 missense variant T/A;C;G snv 0.700 1.000 20 1996 2012
dbSNP: rs63750517
rs63750517
1 1.000 0.080 3 37017590 missense variant T/C snv 0.700 1.000 20 1996 2012
dbSNP: rs63750539
rs63750539
3 0.925 0.160 3 37004426 missense variant C/T snv 0.700 1.000 20 1996 2012
dbSNP: rs63750575
rs63750575
5 0.851 0.160 3 37047550 missense variant T/C snv 0.700 1.000 20 1996 2012
dbSNP: rs63750580
rs63750580
4 0.925 0.160 3 36993659 missense variant A/C;G snv 0.700 1.000 20 1996 2012
dbSNP: rs63750641
rs63750641
2 0.925 0.160 3 37000997 missense variant A/G snv 0.700 1.000 20 1996 2012
dbSNP: rs63750642
rs63750642
1 1.000 0.080 3 37014532 missense variant C/G;T snv 4.0E-06 0.700 1.000 20 1996 2012