Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1212415280
VEGFA
6 43771130 missense variant G/T snv 2.1E-05 2
rs2660852 12 96051770 intergenic variant C/A snv 0.34 3
rs1040411
ATG5
1.000 0.120 6 106150148 intron variant G/A snv 0.47 3
rs4946728
ATG5
1.000 0.120 6 106142488 intron variant A/C snv 0.72 3
rs769483475
CD44
0.925 0.080 11 35229231 missense variant G/A snv 8.0E-06 3
rs3731499
CDC25A
0.925 0.080 3 48184680 missense variant G/A snv 5.7E-05 1.2E-04 3
rs1219211410
CDC25B
0.925 0.080 20 3800494 missense variant T/C snv 3
rs2306536
CHFR
0.925 0.080 12 132847076 missense variant C/T snv 0.18 0.21 3
rs79036859
DAAM1
0.925 0.080 14 59369257 3 prime UTR variant A/G snv 3
rs13423759
ERBB4
0.925 0.080 2 211381247 3 prime UTR variant A/C snv 6.8E-02 3
rs34296044
EXO1
0.925 0.080 1 241885371 frameshift variant C/- delins 3
rs7371084
GTF2A1L ; LHCGR ; STON1-GTF2A1L
0.925 0.120 2 48712814 intron variant T/C snv 0.12 3
rs12881063
LOC107984671 ; LOC105370397
1.000 0.080 14 20788017 downstream gene variant G/C snv 7.4E-02 3
rs41281081
MET
1.000 0.080 7 116796211 3 prime UTR variant G/A snv 2.5E-03 3
rs76322625
MET
1.000 0.080 7 116798111 3 prime UTR variant C/A;T snv 3
rs1235679626
MORC2
0.925 0.080 22 30940834 missense variant C/T snv 1.4E-05 3
rs1207692596
MPO
0.925 0.080 17 58280438 missense variant G/A;T snv 3
rs11121704
MTOR
1 11233902 intron variant C/A;T snv 3
rs1051660
OPRK1
1.000 0.080 8 53251002 synonymous variant C/A;T snv 0.11 3
rs6983561
PCAT1 ; CASC19
0.925 0.080 8 127094635 intron variant A/C snv 0.17 3
rs761872690
PGR ; PGR-AS1
0.925 0.080 11 101128246 synonymous variant G/A snv 2.8E-05 3
rs1370041903
PRKN
0.925 0.120 6 161350185 stop gained G/A snv 3
rs3756824
PRL ; CASC15
0.925 0.080 6 22298508 intron variant C/G;T snv 3
rs370535310
PSAT1
0.925 0.080 9 78304854 missense variant C/T snv 2.1E-05 3
rs773895706
RASGRF1
0.925 0.080 15 79090236 missense variant G/A snv 4.2E-06 3