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: rs10406522
rs10406522
DOCK6
1 1.000 0.080 19 11230959 intron variant T/C snv 0.30 0.700 1.000 1 2018 2018
dbSNP: rs10455872
rs10455872
LPA
33 0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 0.700 1.000 1 2018 2018
dbSNP: rs1830321
rs1830321
TEX41 ; LOC100505498
5 0.827 0.080 2 145067988 intron variant C/T snv 0.40 0.700 1.000 1 2018 2018
dbSNP: rs6702619
rs6702619
LINC01708
4 0.851 0.200 1 99580690 intron variant T/G snv 0.35 0.700 1.000 1 2018 2018
dbSNP: rs7543130
rs7543130
LINC01708
2 0.925 0.080 1 99584229 intron variant C/A snv 0.39 0.700 1.000 1 2018 2018