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: rs185378533
rs185378533
FLJ42102
2 11 71422087 intron variant A/G snv 0.68 0.700 1.000 1 2017 2017
dbSNP: rs12785878
rs12785878
NADSYN1
25 0.677 0.520 11 71456403 intron variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs7938885
rs7938885
NADSYN1
2 11 71458997 non coding transcript exon variant T/C snv 0.59 0.700 1.000 1 2018 2018
dbSNP: rs12800438
rs12800438
NADSYN1
5 1.000 0.080 11 71459957 non coding transcript exon variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs4423214
rs4423214
NADSYN1
2 11 71462208 intron variant C/T snv 0.58 0.700 1.000 1 2017 2017
dbSNP: rs4944062
rs4944062
NADSYN1
2 11 71476248 3 prime UTR variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs3829251
rs3829251
NADSYN1
8 0.851 0.120 11 71483513 intron variant G/A snv 0.21 0.800 1.000 1 2010 2010
dbSNP: rs11234027
rs11234027
NADSYN1
5 0.882 0.080 11 71523061 intron variant G/A snv 0.24 0.700 1.000 1 2010 2010
dbSNP: rs148189294
rs148189294 		2 4 71575200 downstream gene variant G/A snv 2.6E-02 0.700 1.000 1 2017 2017
dbSNP: rs1526692
rs1526692 		2 4 71713007 intergenic variant A/G snv 0.41 0.700 1.000 1 2018 2018
dbSNP: rs17467825
rs17467825 		4 0.925 0.080 4 71739800 downstream gene variant A/G snv 0.22 0.700 1.000 1 2014 2014
dbSNP: rs2282679
rs2282679
GC
38 0.645 0.480 4 71742666 intron variant T/G snv 0.21 0.800 1.000 4 2010 2018
dbSNP: rs3755967
rs3755967
GC
6 0.925 0.080 4 71743681 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs843005
rs843005
GC
2 4 71750610 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs4588
rs4588
GC
53 0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 0.700 1.000 2 2017 2018
dbSNP: rs7041
rs7041
GC
64 0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 0.700 1.000 1 2018 2018
dbSNP: rs1155563
rs1155563
GC
4 0.925 0.080 4 71777771 intron variant T/A;C snv 0.700 1.000 1 2014 2014
dbSNP: rs1607741
rs1607741 		2 4 71853316 intergenic variant G/C snv 0.65 0.700 1.000 1 2017 2017
dbSNP: rs17767445
rs17767445 		2 4 71879550 intergenic variant G/A snv 0.20 0.700 1.000 1 2018 2018
dbSNP: rs79761689
rs79761689 		2 4 72005565 intergenic variant T/C snv 3.7E-02 0.700 1.000 1 2017 2017
dbSNP: rs13107347
rs13107347
NPFFR2
2 4 72109031 intron variant T/C snv 0.32 0.700 1.000 1 2018 2018
dbSNP: rs138485827
rs138485827 		2 4 72166226 intergenic variant C/T snv 5.0E-02 0.700 1.000 1 2017 2017
dbSNP: rs78862524
rs78862524
ADAMTS3
3 4 72305473 intron variant C/A snv 3.9E-02 0.700 1.000 1 2017 2017
dbSNP: rs10485165
rs10485165
LOC105377885
3 6 88403098 intron variant C/G;T snv 0.700 1.000 1 2007 2007
dbSNP: rs10745742
rs10745742
AMDHD1
2 12 95964751 intron variant C/T snv 0.48 0.700 1.000 1 2018 2018