Source: ALL
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: rs267607102
rs267607102
TARDBP
5 0.851 0.120 1 11022196 missense variant A/G snv 0.010 1.000 1 2018 2018
dbSNP: rs28933979
rs28933979
TTR
70 0.587 0.600 18 31592974 missense variant G/A;C snv 1.0E-04 0.010 1.000 1 2001 2001
dbSNP: rs28939711
rs28939711
COX15 ; CUTC
5 0.851 0.120 10 99724057 missense variant G/A snv 3.2E-05 3.5E-05 0.010 1.000 1 2016 2016
dbSNP: rs374651285
rs374651285
ALB
1 4 73406645 missense variant G/A snv 0.010 1.000 1 2019 2019
dbSNP: rs397514662
rs397514662
COX15 ; CUTC
4 0.882 0.120 10 99716419 missense variant A/C;G snv 1.2E-05 0.010 1.000 1 2016 2016
dbSNP: rs398122370
rs398122370
PRNP
4 0.925 0.160 20 4699851 missense variant G/C snv 0.010 1.000 1 2000 2000
dbSNP: rs587777162
rs587777162
EEF1A2
5 0.925 0.040 20 63495972 missense variant C/T snv 0.010 1.000 1 2015 2015
dbSNP: rs62643364
rs62643364
PRNP
7 0.851 0.160 20 4699466 synonymous variant A/G;T snv 4.0E-06; 1.4E-04 0.010 1.000 1 2019 2019
dbSNP: rs74315322
rs74315322
HAX1
3 1.000 0.040 1 154275165 stop gained C/T snv 3.6E-05 0.010 1.000 1 2008 2008
dbSNP: rs749191312
rs749191312
RBBP9
2 1.000 0.080 20 18497075 synonymous variant C/T snv 4.0E-06 0.010 1.000 1 2013 2013
dbSNP: rs756915170
rs756915170
NUP62 ; IL4I1
2 19 49909654 missense variant T/C snv 4.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs771884087
rs771884087
SLPI ; LOC105372630
2 1.000 0.080 20 45253726 synonymous variant T/C snv 0.010 1.000 1 2013 2013
dbSNP: rs80356717
rs80356717
TARDBP
5 0.851 0.120 1 11018836 missense variant A/G snv 0.010 1.000 1 2018 2018
dbSNP: rs80358261
rs80358261
NPC2
3 0.925 0.160 14 74486404 missense variant C/T snv 1.7E-05 1.4E-05 0.010 1.000 1 2005 2005