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: rs10734252
rs10734252 		3 1.000 0.080 11 17383292 non coding transcript exon variant G/A snv 0.71 0.700 1.000 1 2019 2019
dbSNP: rs10795945
rs10795945 		2 1.000 0.080 10 12260608 intergenic variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs10811660
rs10811660 		1 1.000 0.080 9 22134069 intergenic variant G/A snv 0.14 0.700 1.000 1 2019 2019
dbSNP: rs10886863
rs10886863 		1 1.000 0.080 10 121169979 intergenic variant T/C snv 0.82 0.700 1.000 1 2019 2019
dbSNP: rs10938398
rs10938398 		1 1.000 0.080 4 45184122 intergenic variant G/A snv 0.37 0.700 1.000 1 2019 2019
dbSNP: rs10965247
rs10965247 		1 1.000 0.080 9 22132730 downstream gene variant A/G snv 0.15 0.700 1.000 1 2019 2019
dbSNP: rs10968576
rs10968576
LINGO2
10 0.882 0.120 9 28414341 intron variant A/G snv 0.26 0.010 1.000 1 2019 2019
dbSNP: rs11073333
rs11073333
RASGRP1
1 1.000 0.080 15 38528446 intron variant G/A snv 0.76 0.700 1.000 1 2019 2019
dbSNP: rs11073752
rs11073752
NTRK3
2 1.000 0.080 15 87879820 intron variant C/T snv 0.56 0.700 1.000 1 2019 2019
dbSNP: rs11077
rs11077
POLR1C ; XPO5
14 0.732 0.320 6 43523209 3 prime UTR variant T/G snv 0.47 0.010 1.000 1 2019 2019
dbSNP: rs11113776
rs11113776
WSCD2 ; LOC105369965
1 1.000 0.080 12 108219374 intron variant G/A snv 0.44 0.700 1.000 1 2019 2019
dbSNP: rs111248619
rs111248619
KCNQ3
1 1.000 0.080 8 132453251 intron variant G/A snv 3.1E-02 0.700 1.000 1 2019 2019
dbSNP: rs111558778
rs111558778
ADAMTS9-AS2
1 1.000 0.080 3 64763995 intron variant G/A snv 7.0E-06 0.700 1.000 1 2019 2019
dbSNP: rs11199755
rs11199755
LOC105378521
1 1.000 0.080 10 121077345 regulatory region variant C/T snv 8.7E-02 0.700 1.000 1 2019 2019
dbSNP: rs112332300
rs112332300
UBE2E2
1 1.000 0.080 3 23588427 intron variant T/-;TT;TTT;TTTT delins 0.700 1.000 1 2019 2019
dbSNP: rs11255372
rs11255372
LOC105376392
1 1.000 0.080 10 7815130 upstream gene variant G/T snv 0.20 0.010 1.000 1 2019 2019
dbSNP: rs112674299
rs112674299
ATXN7
1 1.000 0.080 3 63996994 intron variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs113547729
rs113547729
ZZEF1
1 1.000 0.080 17 4121530 intron variant G/A snv 3.2E-02 0.700 1.000 1 2019 2019
dbSNP: rs113754532
rs113754532
GLIS3
1 1.000 0.080 9 4286344 missense variant T/C snv 2.5E-04 2.6E-04 0.010 1.000 1 2019 2019
dbSNP: rs11390176
rs11390176
IL13RA1
1 1.000 0.080 X 118781201 intron variant A/-;AA;AAA delins 0.700 1.000 1 2019 2019
dbSNP: rs11410487
rs11410487
ITGA1 ; PELO
1 1.000 0.080 5 52798410 intron variant -/T delins 0.91 0.700 1.000 1 2019 2019
dbSNP: rs11435035
rs11435035
AP3S2 ; ARPIN-AP3S2 ; MIR5094
1 1.000 0.080 15 89850718 non coding transcript exon variant TT/-;T;TTT;TTTT;TTTTT;TTTTTTTTTTTT delins 0.700 1.000 1 2019 2019
dbSNP: rs11466334
rs11466334
TGFB1
1 1.000 0.080 19 41341832 intron variant G/A snv 5.9E-03 2.4E-02 0.700 1.000 1 2019 2019
dbSNP: rs1149833
rs1149833
DLEU1
2 0.925 0.160 13 50176740 intron variant A/T snv 0.47 0.700 1.000 1 2019 2019
dbSNP: rs115321690
rs115321690
CCHCR1
1 1.000 0.080 6 31148749 intron variant A/G;T snv 0.700 1.000 1 2019 2019