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: rs6891174
rs6891174 		2 0.925 0.040 5 173213587 intergenic variant A/G snv 0.73 0.700 1.000 1 2018 2018
dbSNP: rs74154533
rs74154533
NEURL1
1 1.000 10 103547967 intron variant G/A snv 0.17 0.700 1.000 1 2018 2018
dbSNP: rs761740955
rs761740955
FGB
5 0.827 0.200 4 154566637 missense variant A/G snv 4.0E-06 0.010 1.000 1 2017 2017