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: rs61752416
rs61752416
1 1.000 1 94042828 missense variant T/G snv 0.800 1.000 22 1997 2017
dbSNP: rs61749414
rs61749414
3 0.882 0.080 1 94062611 stop gained G/A;T snv 0.800 1.000 21 1997 2017
dbSNP: rs281865404
rs281865404
4 0.851 0.080 1 94014675 missense variant GG/CA mnv 0.710 1.000 20 1997 2014
dbSNP: rs61749428
rs61749428
1 1.000 1 94056692 missense variant C/T snv 7.0E-06 0.800 1.000 20 1997 2017
dbSNP: rs61753028
rs61753028
1 1.000 1 94015763 missense variant A/G snv 0.800 1.000 20 1997 2017
dbSNP: rs281865397
rs281865397
1 1.000 1 94103015 missense variant C/G snv 0.700 1.000 19 1997 2014
dbSNP: rs281865402
rs281865402
1 1.000 1 94029446 missense variant T/C snv 2.1E-05 0.700 1.000 19 1997 2014
dbSNP: rs281865405
rs281865405
1 1.000 1 94000836 missense variant T/C snv 0.700 1.000 19 1997 2014
dbSNP: rs61748524
rs61748524
1 1.000 1 94111566 missense variant G/C snv 0.700 1.000 19 1997 2014
dbSNP: rs61748526
rs61748526
1 1.000 1 94111517 missense variant A/C snv 1.4E-05 0.800 1.000 19 1997 2014
dbSNP: rs61748527
rs61748527
1 1.000 1 94111510 missense variant A/G;T snv 0.700 1.000 19 1997 2014
dbSNP: rs61748530
rs61748530
1 1.000 1 94111442 missense variant A/G snv 1.4E-05 0.700 1.000 19 1997 2014
dbSNP: rs61748544
rs61748544
1 1.000 1 94080678 missense variant G/T snv 0.700 1.000 19 1997 2014
dbSNP: rs61748548
rs61748548
1 1.000 1 94080559 missense variant A/C;G snv 0.800 1.000 19 1997 2014
dbSNP: rs61749429
rs61749429
1 1.000 1 94056689 missense variant C/G;T snv 0.700 1.000 19 1997 2014
dbSNP: rs61749432
rs61749432
1 1.000 1 94055308 missense variant A/G snv 0.700 1.000 19 1997 2014
dbSNP: rs61749436
rs61749436
1 1.000 1 94055146 missense variant C/T snv 0.700 1.000 19 1997 2014
dbSNP: rs61749448
rs61749448
1 1.000 1 94046967 missense variant T/C snv 7.0E-06 0.700 1.000 19 1997 2014
dbSNP: rs61749456
rs61749456
1 1.000 1 94044622 missense variant A/C snv 7.0E-06 0.700 1.000 19 1997 2014
dbSNP: rs61750060
rs61750060
1 1.000 1 94043435 missense variant T/C snv 0.700 1.000 19 1997 2014
dbSNP: rs61750122
rs61750122
1 1.000 1 94041396 missense variant G/T snv 7.0E-06 0.700 1.000 19 1997 2014
dbSNP: rs61750128
rs61750128
1 1.000 1 94037209 missense variant A/G snv 0.700 1.000 19 1997 2014
dbSNP: rs61750133
rs61750133
1 1.000 1 94031033 missense variant G/A snv 0.700 1.000 19 1997 2014
dbSNP: rs61750134
rs61750134
1 1.000 1 94031026 missense variant C/A snv 0.700 1.000 19 1997 2014
dbSNP: rs61750151
rs61750151
1 1.000 1 94025014 missense variant A/G snv 0.700 1.000 19 1997 2014