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: rs10415749
rs10415749
CNN1
1 19 11541905 intron variant T/G snv 1.4E-02 0.700 1.000 1 2016 2016
dbSNP: rs16950081
rs16950081
LINC01169
1 15 66630879 intron variant G/A snv 5.3E-02 0.700 1.000 1 2016 2016
dbSNP: rs6042935
rs6042935
MACROD2
1 20 14816926 intron variant A/G snv 8.2E-02 0.700 1.000 1 2016 2016
dbSNP: rs71632123
rs71632123
CACNA1E
1 1 181776565 intron variant C/A snv 3.1E-02 0.700 1.000 1 2016 2016
dbSNP: rs8060581
rs8060581
LOC102724084 ; LOC105371357
1 16 80158708 intron variant G/C snv 0.16 0.700 1.000 1 2013 2013
dbSNP: rs8178822
rs8178822
APOH
1 17 66229411 5 prime UTR variant G/T snv 6.3E-02 6.7E-02 0.700 1.000 1 2016 2016
dbSNP: rs8178848
rs8178848
APOH
1 17 66219505 intron variant G/A snv 7.4E-02 0.700 1.000 1 2016 2016
dbSNP: rs9910950
rs9910950
CEP112
1 17 66135592 intron variant A/G snv 5.8E-02 0.700 1.000 1 2016 2016