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: rs34354898
rs34354898 		1 1.000 0.080 6 87129144 intergenic variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs346785
rs346785
QRICH2
1 1.000 0.080 17 76287688 intron variant T/C snv 0.53 0.700 1.000 1 2016 2016
dbSNP: rs35436
rs35436 		5 1.000 0.080 12 115116718 intergenic variant C/T snv 0.40 0.700 1.000 1 2018 2018
dbSNP: rs360139
rs360139 		1 1.000 0.080 11 9753544 upstream gene variant A/G snv 0.62 0.700 1.000 1 2018 2018
dbSNP: rs3733655
rs3733655
PCDH7
1 1.000 0.080 4 31144396 3 prime UTR variant A/G snv 0.48 0.700 1.000 1 2016 2016
dbSNP: rs42039
rs42039
CDK6
3 1.000 0.080 7 92615108 3 prime UTR variant C/T snv 0.19 0.19 0.700 1.000 1 2018 2018
dbSNP: rs4444878
rs4444878
F11-AS1
7 0.851 0.120 4 186292729 intron variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs4471613
rs4471613
ALDH1A2
3 1.000 0.080 15 58259495 intron variant G/A snv 4.3E-02 0.700 1.000 1 2015 2015
dbSNP: rs4932370
rs4932370 		2 1.000 0.080 15 90861475 intergenic variant G/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs4959130
rs4959130 		2 1.000 0.080 6 1356681 intergenic variant G/A snv 9.8E-02 0.700 1.000 1 2018 2018
dbSNP: rs4962153
rs4962153
ADAMTS13 ; CACFD1
9 0.925 0.120 9 133458632 intron variant A/G snv 0.79 0.700 1.000 1 2017 2017
dbSNP: rs5752326
rs5752326
HPS4
1 1.000 0.080 22 26448024 intron variant C/G;T snv 0.700 1.000 1 2015 2015
dbSNP: rs59920395
rs59920395 		1 1.000 0.080 5 3650229 intergenic variant C/T snv 6.0E-02 0.700 1.000 1 2016 2016
dbSNP: rs60942712
rs60942712 		5 0.882 0.120 3 88998609 intergenic variant G/T snv 7.9E-02 0.700 1.000 1 2016 2016
dbSNP: rs61937565
rs61937565 		1 1.000 0.080 12 38997354 upstream gene variant T/C snv 0.11 0.700 1.000 1 2019 2019
dbSNP: rs61937587
rs61937587 		1 1.000 0.080 12 39004369 intergenic variant G/A snv 0.15 0.700 1.000 1 2019 2019
dbSNP: rs6565653
rs6565653
SLC26A11
1 1.000 0.080 17 80227984 intron variant T/A;G snv 4.4E-06; 0.63 0.700 1.000 1 2016 2016
dbSNP: rs6764132
rs6764132 		2 1.000 0.080 3 39747400 regulatory region variant C/T snv 2.7E-02 0.700 1.000 1 2016 2016
dbSNP: rs6825454
rs6825454 		3 1.000 0.080 4 154580036 downstream gene variant T/C snv 0.25 0.700 1.000 1 2018 2018
dbSNP: rs701230
rs701230
KCNK1
1 1.000 0.080 1 233635529 intron variant C/G snv 0.18 0.700 1.000 1 2016 2016
dbSNP: rs704341
rs704341
PTPRG
2 1.000 0.080 3 61963062 intron variant G/A snv 0.11 0.700 1.000 1 2015 2015
dbSNP: rs7082237
rs7082237
C10orf143
1 1.000 0.080 10 130091533 intron variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs72798544
rs72798544
COX7A2L
5 0.882 0.120 2 42372465 intron variant T/G snv 1.3E-02 0.700 1.000 1 2016 2016
dbSNP: rs7304841
rs7304841
PDE3A
2 1.000 0.080 12 20424659 intron variant A/C;G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs73712231
rs73712231 		1 1.000 0.080 8 137203404 intergenic variant C/T snv 9.9E-02 0.700 1.000 1 2019 2019