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: rs10995190
rs10995190
ZNF365
4 0.882 0.080 10 62518923 intron variant G/A snv 0.16 0.700 1.000 1 2011 2011
dbSNP: rs1248032
rs1248032
LOC105369998
1 12 114442904 intergenic variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs1265507
rs1265507
LOC105369998
3 0.925 0.080 12 114430333 regulatory region variant A/G snv 0.52 0.700 1.000 1 2012 2012
dbSNP: rs12838671
rs12838671 		1 X 4216809 intergenic variant C/A;G snv 0.700 1.000 1 2012 2012
dbSNP: rs2363842
rs2363842 		1 X 4299727 intergenic variant T/C snv 0.50 0.700 1.000 1 2012 2012
dbSNP: rs2551389
rs2551389
LOC105369998
1 12 114419921 regulatory region variant A/G snv 0.48 0.700 1.000 1 2012 2012
dbSNP: rs2686573
rs2686573
LOC105369998
1 12 114441748 intergenic variant A/G snv 0.73 0.700 1.000 1 2012 2012
dbSNP: rs5961472
rs5961472 		1 X 4218922 intergenic variant T/C snv 0.700 1.000 1 2012 2012
dbSNP: rs6529954
rs6529954 		1 X 4266308 intergenic variant A/G snv 0.700 1.000 1 2012 2012