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: rs114864815
rs114864815
HCP5
1 6 31461210 intron variant C/T snv 0.700 1.000 1 2015 2015
dbSNP: rs142765674
rs142765674
LINC02785
1 1 108070308 intron variant A/G snv 4.7E-03 0.700 1.000 1 2019 2019
dbSNP: rs144721899
rs144721899
TMC7
1 16 18993889 intron variant A/G snv 3.4E-03 0.700 1.000 1 2019 2019
dbSNP: rs147482218
rs147482218
LRRC32
1 11 76667642 intron variant T/G snv 7.9E-03 0.700 1.000 1 2019 2019
dbSNP: rs17199328
rs17199328
HLA-B
1 6 31354618 non coding transcript exon variant A/C;G;T snv 4.0E-06; 9.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs537841689
rs537841689 		1 12 90550058 intergenic variant C/T snv 3.6E-04 0.700 1.000 1 2019 2019
dbSNP: rs541558502
rs541558502
FAM110B
1 8 58095231 intron variant G/A snv 1.0E-03 0.700 1.000 1 2019 2019
dbSNP: rs75640364
rs75640364
HCP5
1 6 31465789 non coding transcript exon variant G/C snv 6.1E-02 0.700 1.000 1 2019 2019
dbSNP: rs765885335
rs765885335 		1 6 104245432 intergenic variant A/G snv 3.6E-04 0.700 1.000 1 2019 2019
dbSNP: rs9810195
rs9810195 		1 3 193028537 regulatory region variant A/G snv 0.16 0.700 1.000 1 2019 2019