Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12921862
AXIN1
0.763 0.200 16 331927 intron variant C/A snv 0.18 10
rs870142
STX18-AS1
0.851 0.120 4 4646320 intron variant C/G;T snv 7
rs1531070
MAML3
0.851 0.120 4 139874173 intron variant G/A snv 0.30 6
rs9909104
SHMT1
0.882 0.200 17 18344707 intron variant T/C snv 0.30 4
rs4720169
TBX20
1.000 0.040 7 35247689 intron variant G/A snv 0.53 2
rs1176869
LOC105370467
14 40807221 intron variant C/G snv 0.19 1
rs11895588
LRP1B
2 141204588 intron variant G/T snv 0.12 1
rs12438477
MTHFS ; ST20-MTHFS
15 79885941 intron variant C/A;T snv 1
rs1245314 14 27023434 intron variant A/G;T snv 1
rs492842
DMGDH ; BHMT
5 79114164 intron variant C/T snv 0.59 1
rs542852
DMGDH ; BHMT
5 79113573 intron variant T/C snv 0.63 1
rs66678247
LOC107986115
3 114227412 intron variant T/C snv 9.9E-02 1
rs7294985
MGST1
12 16349610 intron variant A/G;T snv 1
rs2474937 0.851 0.120 1 118360355 intergenic variant A/G snv 0.25 6
rs17111230 14 40922047 intergenic variant G/C snv 0.56 1
rs56409046 6 9320073 intergenic variant C/T snv 0.27 1
rs2844660 6 30855983 regulatory region variant T/C snv 7.9E-02 1
rs75661265 8 59275232 regulatory region variant C/T snv 0.11 1
rs1057518422
TAB2
0.851 0.240 6 149378954 stop gained C/T snv 7
rs114878910
EXOSC3
0.882 0.080 9 37784894 stop gained G/A;C snv 8.6E-06; 3.1E-04 4
rs763679435
LOC101928462 ; TSHR
0.882 0.120 14 81143883 stop gained C/T snv 4.0E-06 2.1E-05 4
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135