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: rs67072384
rs67072384
ARAP1
2 0.925 0.080 11 72739679 intron variant C/T snv 0.14 0.700 1.000 1 2014 2014
dbSNP: rs75853687
rs75853687
LINC01847
2 0.925 0.080 5 159850278 intron variant G/A snv 1.7E-02 0.700 1.000 1 2018 2018
dbSNP: rs202229101
rs202229101
GP9
2 0.925 3 129062107 missense variant C/T snv 9.5E-04 8.7E-04 0.010 1.000 1 2017 2017