Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2498804
LOC102723342 ; SIVA1 ; LOC107987209
0.827 0.160 14 104766758 intron variant C/A;T snv 0.40 0.33 8
rs3803300
ZBTB42
0.827 0.120 14 104803442 3 prime UTR variant T/A;C snv 6
rs778293 0.807 0.120 13 105516850 intergenic variant C/A;T snv 7
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs602201
MPPE1 ; GNAL
0.925 0.120 18 11882269 3 prime UTR variant T/A snv 0.34 2
rs593713
MPPE1
0.925 0.120 18 11887658 intron variant G/A snv 0.42 2
rs3974590
MPPE1
0.925 0.120 18 11892846 intron variant A/G snv 0.35 2
rs3786285
IMPA2
0.925 0.120 18 12008848 intron variant A/C;G snv 2
rs613993
IMPA2
0.925 0.120 18 12028581 non coding transcript exon variant A/G snv 0.33 2
rs2230912
P2RX7 ; LOC105370032
0.752 0.280 12 121184393 missense variant A/G snv 0.13 0.12 16
rs11199993
FGFR2
0.925 0.120 10 121531750 intron variant G/C snv 4.8E-02 2
rs78089757 0.882 0.120 10 125424260 intergenic variant G/A snv 9.9E-03 3
rs28364997
SLC6A3
0.807 0.120 5 1403013 missense variant G/A snv 5.3E-04 5.8E-04 9
rs6413429
SLC6A3
0.925 0.120 5 1446912 upstream gene variant C/A snv 6.1E-02 2
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs9371601
SYNE1
0.790 0.120 6 152469438 intron variant G/T snv 0.46 8
rs41084
SGCD
0.925 0.120 5 156118554 intron variant A/T snv 0.45 2
rs187269
GABRB2
0.827 0.160 5 161329618 3 prime UTR variant A/G snv 0.34 6
rs2546620
GABRB2
0.882 0.120 5 161332120 intron variant T/C snv 0.15 3
rs7597593
ZNF804A
0.827 0.160 2 184668853 intron variant T/C snv 0.53 6
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs1938516
ERVMER61-1
0.925 0.120 1 187433789 intron variant T/A snv 5.7E-02 2
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs165599
ARVCF ; COMT
0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27