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: rs6589075
rs6589075
LINC02713
1 11 97888820 intron variant C/T snv 9.2E-02 0.700 1.000 1 2018 2018
dbSNP: rs870306
rs870306
IGF1R
1 15 98776578 intron variant T/G snv 0.12 0.700 1.000 1 2018 2018
dbSNP: rs405509
rs405509
APOE
30 0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 0.010 1.000 1 2015 2015