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: rs12598357
rs12598357 		15 0.724 0.240 16 28329624 intergenic variant A/G snv 0.43 0.700 1.000 1 2015 2015
dbSNP: rs12863738
rs12863738 		14 0.724 0.240 X 136949968 intron variant C/T snv 0.16 0.700 1.000 1 2015 2015
dbSNP: rs12928404
rs12928404
ATXN2L
15 0.724 0.240 16 28835925 splice region variant T/C snv 0.44 0.45 0.700 1.000 1 2015 2015
dbSNP: rs12928822
rs12928822
RMI2 ; LOC105371082
5 0.882 0.200 16 11310036 intron variant C/T snv 0.13 0.700 1.000 1 2011 2011
dbSNP: rs12980063
rs12980063
CPT1C
4 0.882 19 49693735 intron variant A/G snv 0.48 0.700 1.000 1 2019 2019
dbSNP: rs13003464
rs13003464
PUS10
7 0.827 0.200 2 60959694 intron variant A/G snv 0.50 0.700 1.000 1 2011 2011
dbSNP: rs13010713
rs13010713
LINC01934
5 0.882 0.200 2 181131318 intron variant A/C;G snv 0.700 1.000 1 2011 2011
dbSNP: rs13031237
rs13031237
REL
3 1.000 0.120 2 60908994 intron variant G/T snv 0.25 0.700 1.000 1 2011 2011
dbSNP: rs13098911
rs13098911
CCR3
5 0.882 0.200 3 46193709 intron variant C/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs13119723
rs13119723
KIAA1109
8 0.807 0.280 4 122297158 intron variant A/G snv 0.10 0.700 1.000 1 2011 2011
dbSNP: rs1320344
rs1320344
C12orf42
4 0.882 12 103493699 intron variant A/G snv 0.64 0.700 1.000 1 2019 2019
dbSNP: rs13299616
rs13299616
PSMD5 ; CUTALP
4 0.882 9 120832525 intron variant T/C snv 0.50 0.700 1.000 1 2019 2019
dbSNP: rs13314993
rs13314993
LOC105377022
5 0.882 0.200 3 32973977 regulatory region variant G/C;T snv 0.700 1.000 1 2011 2011
dbSNP: rs13315591
rs13315591
FAM107A ; LOC107984079
4 0.925 0.160 3 58571114 intron variant T/C snv 0.15 0.700 1.000 1 2011 2011
dbSNP: rs1332099
rs1332099 		14 0.724 0.240 10 99538694 downstream gene variant T/C;G snv 0.700 1.000 1 2015 2015
dbSNP: rs13380830
rs13380830
RAB5C
4 0.882 17 42145640 intron variant C/G snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs1355208
rs1355208 		2 2 30222456 intergenic variant A/G snv 0.65 0.700 1.000 1 2011 2011
dbSNP: rs142647938
rs142647938
KCNH7
4 0.882 2 162516642 intron variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1443438
rs1443438
PTCSC2
8 0.827 0.080 9 97787746 intron variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs145268310
rs145268310 		4 0.882 3 12269274 regulatory region variant G/C snv 9.9E-02 0.700 1.000 1 2019 2019
dbSNP: rs1464510
rs1464510
LPP
9 0.807 0.280 3 188394766 intron variant C/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs1530687
rs1530687
ARHGAP31
4 0.882 3 119395668 intron variant G/A snv 0.46 0.700 1.000 1 2019 2019
dbSNP: rs1534430
rs1534430
MIR3681HG
5 0.851 0.040 2 12504610 intron variant C/T snv 0.35 0.700 1.000 1 2019 2019
dbSNP: rs1549922
rs1549922 		4 0.882 5 159304540 intergenic variant G/A snv 0.56 0.700 1.000 1 2019 2019
dbSNP: rs1689510
rs1689510
SUOX
16 0.724 0.240 12 56002984 non coding transcript exon variant G/C snv 0.25 0.700 1.000 1 2015 2015