Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507520
PTPN11
0.658 0.520 12 112453279 missense variant G/C;T snv 39
rs2295080
MTOR
0.695 0.320 1 11262571 upstream gene variant G/C;T snv 20
rs1020608187
SDS
1.000 0.120 12 113398843 missense variant C/G snv 7.0E-06 1
rs35134728
C1orf167 ; MTHFR
0.882 0.120 1 11787277 3 prime UTR variant -/AGA delins 3
rs3737966
C1orf167 ; MTHFR
0.882 0.120 1 11787702 3 prime UTR variant C/T snv 0.55 3
rs4846049
C1orf167 ; MTHFR
0.776 0.360 1 11790308 3 prime UTR variant T/A;G snv 11
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs200890679
MTHFR
0.790 0.240 1 11795191 missense variant C/A;G snv 1.8E-04 2.0E-04 7
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs525549
KMT2A
0.882 0.120 11 118487353 intron variant T/A snv 0.33 3
rs6589664
TMEM25
0.882 0.120 11 118534089 synonymous variant G/A snv 0.30 0.27 3
rs724159947
ETV6
0.851 0.120 12 11869601 missense variant C/T snv 6
rs786205155
ETV6
0.882 0.120 12 11884481 missense variant T/C snv 4
rs1573613
ETV6
0.882 0.120 12 11894684 3 prime UTR variant T/C snv 0.48 3
rs757874631
CBL
0.882 0.120 11 119278211 missense variant T/A;C snv 4
rs1057519743
CRLF2
0.827 0.120 Y 1196852 missense variant A/C snv 6
rs543412
MIR100HG ; MIR100 ; MIR10526
0.925 0.120 11 122152219 intron variant C/T snv 2.0E-05; 0.32 0.32 2
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 23
rs16917496
KMT5A
0.689 0.360 12 123409283 3 prime UTR variant C/G;T snv 21
rs35837782
LHPP
0.925 0.120 10 124604740 intron variant A/G snv 0.63 2
rs7039798
FPGS
0.882 0.120 9 127794947 intron variant G/A;C snv 3
rs1544105
FPGS
0.851 0.200 9 127800446 intron variant C/T snv 0.48 4
rs10106
FPGS
0.851 0.200 9 127813796 3 prime UTR variant T/C snv 0.45 4