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: rs1065483
rs1065483
NUP88 ; RABEP1
1 17 5381475 synonymous variant G/A snv 0.53 0.51 0.700 1.000 1 2012 2012
dbSNP: rs10748016
rs10748016 		1 12 65138965 downstream gene variant A/T snv 0.57 0.700 1.000 1 2012 2012
dbSNP: rs10768983
rs10768983
HSD17B12
1 11 43818385 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs10777181
rs10777181
POC1B
1 12 89514850 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs10799505
rs10799505 		1 1 224163321 downstream gene variant C/T snv 0.41 0.700 1.000 1 2012 2012
dbSNP: rs10805888
rs10805888
LINC01331
1 5 74489722 intron variant A/G snv 0.36 0.700 1.000 1 2012 2012
dbSNP: rs10828723
rs10828723
PRTFDC1
1 10 24916129 intron variant T/C snv 0.26 0.700 1.000 1 2016 2016
dbSNP: rs10844372
rs10844372 		1 12 9663306 upstream gene variant G/C snv 0.68 0.700 1.000 1 2012 2012
dbSNP: rs10844639
rs10844639 		1 12 9736166 upstream gene variant C/T snv 0.31 0.700 1.000 1 2018 2018
dbSNP: rs10844706
rs10844706
CD69
1 12 9757536 intron variant C/A snv 0.34 0.700 1.000 1 2016 2016
dbSNP: rs10867411
rs10867411
TLE4
1 9 79683075 intron variant A/G snv 0.52 0.700 1.000 1 2016 2016
dbSNP: rs10886369
rs10886369 		1 10 119024129 intron variant A/G snv 0.31 0.700 1.000 1 2012 2012
dbSNP: rs10900594
rs10900594 		1 1 204501001 intergenic variant G/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10901450
rs10901450
UROS
1 10 125820725 intron variant G/C snv 0.41 0.700 1.000 1 2012 2012
dbSNP: rs11016797
rs11016797 		1 10 129451806 intergenic variant G/C snv 0.43 0.700 1.000 1 2012 2012
dbSNP: rs11024625
rs11024625
GTF2H1 ; LOC105376577
1 11 18350013 intron variant A/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs11064237
rs11064237
NCAPD2
1 12 6504990 intron variant T/C snv 0.34 0.700 1.000 1 2012 2012
dbSNP: rs11068277
rs11068277
FBXW8 ; LOC100506551
1 12 116986701 non coding transcript exon variant T/A snv 0.67 0.700 1.000 1 2012 2012
dbSNP: rs11077815
rs11077815
UBE2O
1 17 76393809 intron variant T/C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs11149841
rs11149841
GABARAPL2
1 16 75568899 intron variant G/T snv 0.17 0.700 1.000 1 2012 2012
dbSNP: rs11168249
rs11168249
HDAC7
9 0.807 0.120 12 47814585 intron variant T/C snv 0.50 0.700 1.000 1 2016 2016
dbSNP: rs11171739
rs11171739
ERBB3
10 0.807 0.320 12 56076841 5 prime UTR variant C/T snv 0.49 0.700 1.000 1 2012 2012
dbSNP: rs11172333
rs11172333
EEF1AKMT3
1 12 57776552 intron variant A/G snv 0.26 0.700 1.000 1 2012 2012
dbSNP: rs1120277
rs1120277 		1 14 77011321 regulatory region variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs11211101
rs11211101
TESK2
1 1 45383639 intron variant G/C snv 0.27 0.700 1.000 1 2012 2012