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: rs115256310
rs115256310
LOC105379028
1 5 72103864 intron variant A/G snv 1.2E-02 0.700 1.000 1 2017 2017
dbSNP: rs11903143
rs11903143
ALK
1 2 29369594 intron variant A/G snv 0.28 0.700 1.000 1 2017 2017
dbSNP: rs143158039
rs143158039
SLC5A8
1 12 101155156 downstream gene variant A/-;AA;AAA delins 0.700 1.000 1 2017 2017
dbSNP: rs145756094
rs145756094
LINGO2
1 9 29106807 intergenic variant C/A;G snv 0.700 1.000 1 2017 2017
dbSNP: rs2324653
rs2324653 		1 4 25056040 intergenic variant G/C snv 0.52 0.700 1.000 1 2017 2017
dbSNP: rs5167
rs5167
APOC2 ; APOC4 ; APOC4-APOC2
7 1.000 0.040 19 44945208 missense variant T/A;G snv 3.6E-05; 0.39 0.700 1.000 1 2017 2017
dbSNP: rs76287671
rs76287671
ZNF428 ; LOC105372411
1 19 43618144 intron variant C/T snv 0.13 0.700 1.000 1 2017 2017