Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11196067
VTI1A
0.752 0.160 10 112709306 intron variant A/T snv 0.32 10
rs11196172
TCF7L2
0.708 0.200 10 112967084 intron variant G/A snv 0.13 10
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 79
rs7904519
TCF7L2
0.763 0.240 10 113014168 intron variant A/G snv 0.55 8
rs648044
ZBTB16 ; LOC101928875
0.882 0.040 11 114160077 non coding transcript exon variant A/G;T snv 2
rs17138945
MET
1.000 0.040 7 116703812 intron variant T/G snv 7.3E-02 1
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 92
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs498872
PHLDB1
0.776 0.240 11 118606652 5 prime UTR variant A/G;T snv 8
rs11603023
PHLDB1
0.925 0.120 11 118615352 intron variant T/C snv 0.57 1
rs2236661
PHLDB1
1.000 0.040 11 118628678 intron variant C/G snv 0.24 0.20 1
rs494560
PHLDB1
1.000 0.040 11 118650844 non coding transcript exon variant A/G snv 0.57 1
rs17748
TREH ; PHLDB1
0.827 0.080 11 118657714 3 prime UTR variant C/T snv 0.18 5
rs643788
H2AX ; DPAGT1
1.000 0.040 11 119097048 missense variant T/C snv 0.42 0.38 1
rs41278075
ANXA5
1.000 0.040 4 121669758 intron variant G/A snv 0.23 0.18 1
rs2306420
ANXA5
1.000 0.040 4 121670320 intron variant G/A snv 0.21 1
rs117677079
ANXA5
0.882 0.040 4 121673909 intron variant T/C snv 8.3E-03 3
rs145619195
ANXA5
1.000 0.040 4 121674585 intron variant T/C snv 9.4E-04 1
rs2306415
ANXA5
1.000 0.040 4 121696476 intron variant C/G snv 0.16 1
rs1131239
ANXA5
1.000 0.040 4 121696590 5 prime UTR variant G/A;C;T snv 0.12 0.17 1
rs781754593
TNFRSF1B
1.000 0.040 1 12202039 missense variant A/G snv 4.2E-06 1
rs1339499
MAPKAP1
1.000 0.040 9 125644174 intron variant T/C snv 0.29 1
rs473426
MAPKAP1
1.000 0.040 9 125644709 intron variant G/C snv 0.44 1
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 40