Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13306556
MTHFR
1 11792053 intron variant C/T snv 0.10 2
rs13306561
MTHFR ; CLCN6
1 11805747 5 prime UTR variant A/G snv 0.18 2
rs6541006
MTHFR
1 11797469 intron variant A/G;T snv 2
rs1360182594
MTHFR
1 11790755 synonymous variant G/A snv 4.0E-06 1
rs17037388
MTHFR
1 11797979 intron variant A/G snv 0.17 1
rs3818762
MTHFR
1 11790946 intron variant G/C snv 0.26; 1.7E-03 0.23 1
rs45553335
MTHFR
1 11798900 intron variant T/C snv 0.14 1
rs576853093
MTHFR
1 11790946 intron variant -/C;CACACACACACAC ins 6.2E-03 1
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
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs9651118
MTHFR
0.683 0.480 1 11802157 intron variant T/C snv 0.18 20
rs4846048
MTHFR ; C1orf167
0.752 0.280 1 11786195 3 prime UTR variant G/A snv 0.67 10
rs4846049
C1orf167 ; MTHFR
0.776 0.360 1 11790308 3 prime UTR variant T/A;G snv 11
rs1476413
MTHFR
0.790 0.360 1 11792243 intron variant C/G;T snv 4.0E-06; 0.26 0.23 10
rs200890679
MTHFR
0.790 0.240 1 11795191 missense variant C/A;G snv 1.8E-04 2.0E-04 7
rs768873896
MTHFR
0.790 0.160 1 11794822 missense variant C/G;T snv 8.0E-06; 2.4E-05 7
rs1200746244
MTHFR
0.807 0.080 1 11801287 missense variant C/T snv 4.0E-06 7.0E-06 11
rs1255283120
MTHFR
0.807 0.160 1 11792345 missense variant G/A snv 4.0E-06 7.0E-06 7
rs2274976
MTHFR
0.807 0.320 1 11790870 missense variant C/T snv 5.6E-02 4.2E-02 7
rs3753584
MTHFR ; CLCN6
0.827 0.080 1 11804529 5 prime UTR variant T/C snv 0.14 10
rs1194897557
MTHFR
0.827 0.240 1 11796276 missense variant A/G snv 8.0E-06 7
rs55763075
MTHFR ; C1orf167
0.827 0.120 1 11790377 3 prime UTR variant C/T snv 2.1E-05 6
rs12121543
MTHFR
0.851 0.240 1 11794614 intron variant C/A snv 0.21 4