Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3832406
MTHFD1L
0.925 6 150898848 intron variant -/A;ATA;ATTATG ins 5.8E-05; 4.3E-05 2.1E-05 3
rs10925260
MTR
1 236884786 intron variant A/C snv 0.56 1
rs777628969
CALR ; MIR6515
19 12940603 missense variant A/C snv 8.0E-06 1
rs3755166
LRP2
1.000 0.080 2 169363371 upstream gene variant A/C;G snv 4
rs34059106
VANGL1
1 115684037 missense variant A/C;G snv 4.0E-03; 4.0E-06 1.7E-02 1
rs3808553
FZD6
8 103325139 missense variant A/C;G snv 0.47 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1801394
FASTKD3 ; MTRR
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1039659576
MTR
0.689 0.520 1 236803473 missense variant A/G snv 21
rs1950902
MTHFD1
0.776 0.240 14 64415662 missense variant A/G snv 0.83 0.83 11
rs737865
TXNRD2 ; COMT
0.763 0.240 22 19942598 intron variant A/G snv 0.23 11
rs202676
FOLH1
0.851 0.160 11 49206068 stop lost A/G snv 0.28 0.33 7
rs162036
MTRR
0.827 0.200 5 7885846 missense variant A/G snv 0.18 0.21 6
rs12132032
PRKACB
1.000 0.080 1 84100906 intron variant A/G snv 0.41 2
rs17719944
SLC46A1 ; SARM1
17 28402435 3 prime UTR variant A/G snv 5.8E-02 1
rs751421713
MTHFD1L
6 151013801 missense variant A/G snv 8.0E-06 1
rs7646
MIR12131 ; MTHFD1L
6 151101614 3 prime UTR variant A/G;T snv 0.22 1
rs562920966
DACT1
14 58645694 missense variant A/T snv 8.0E-06 1
rs594631
PRKACB ; LOC107985046
1 84220882 intron variant A/T snv 0.31 1
rs34396413
TFAP2A
0.925 0.160 6 10400802 intron variant AGA/- delins 6.8E-02 6.9E-02 3
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32
rs775144154
SLC19A1
0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 38
rs1212671656
TUBGCP2
10 133297981 missense variant C/G snv 4.0E-06 1
rs1257122540
SEC24B
4 109539620 missense variant C/G snv 7.0E-06 1