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: rs117834366
rs117834366
CNTNAP2
2 0.925 0.120 7 147937799 intron variant G/A snv 1.2E-02 0.700 1.000 1 2019 2019
dbSNP: rs12007229
rs12007229 		1 1.000 0.120 X 67528513 upstream gene variant C/A snv 0.11 0.700 1.000 1 2012 2012
dbSNP: rs2497931
rs2497931 		1 1.000 0.120 X 67436434 intergenic variant A/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs26906
rs26906
RASGRF2
1 1.000 0.120 5 81069068 intron variant T/C snv 0.86 0.700 1.000 1 2012 2012
dbSNP: rs429358
rs429358
APOE
66 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 0.700 1.000 1 2019 2019
dbSNP: rs4485213
rs4485213 		1 1.000 0.120 13 105256524 intergenic variant C/T snv 0.19 0.700 1.000 1 2012 2012
dbSNP: rs290227
rs290227
SYK
1 1.000 0.120 9 90874382 intron variant G/A snv 0.30 0.810 1.000 1 2013 2013