Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2835931
KCNJ6
1.000 0.120 21 37749345 intron variant C/A;T snv 4
rs477145
TIAM1
1.000 0.120 21 31390097 intron variant C/A;T snv 4
rs7668666
TLR3
1.000 4 186080138 intron variant C/A;T snv 4
rs1040411
ATG5
1.000 0.120 6 106150148 intron variant G/A snv 0.47 3
rs1051660
OPRK1
1.000 0.080 8 53251002 synonymous variant C/A;T snv 0.11 3
rs1196644309
TXNIP
1.000 0.080 1 145995155 missense variant G/A snv 3
rs12881063
LOC107984671 ; LOC105370397
1.000 0.080 14 20788017 downstream gene variant G/C snv 7.4E-02 3
rs200081710
TNIP3
1.000 0.120 4 121154648 missense variant T/C snv 7.0E-06 3
rs41281081
MET
1.000 0.080 7 116796211 3 prime UTR variant G/A snv 2.5E-03 3
rs4946728
ATG5
1.000 0.120 6 106142488 intron variant A/C snv 0.72 3
rs754854286
ZEB1
1.000 0.120 10 31520432 missense variant G/C snv 3
rs76322625
MET
1.000 0.080 7 116798111 3 prime UTR variant C/A;T snv 3
rs10420252
COX6B1
1.000 0.080 19 35648270 upstream gene variant G/A snv 9.7E-02 2
rs11246050
NLRP6
1.000 0.080 11 284257 synonymous variant G/A;C snv 0.16; 4.0E-06 2
rs1340026226
AR
1.000 0.080 X 67711662 missense variant G/A snv 9.5E-06 2
rs1347591
NUP93
1.000 0.080 16 56834788 intron variant A/G snv 0.47 0.47 2
rs140451238
ITK
1.000 0.080 5 157208978 synonymous variant T/C snv 1.6E-04 7.8E-04 2
rs1410727652
SLC22A3
1.000 0.080 6 160348669 missense variant C/T snv 7.0E-06 2
rs2118593
RYBP
1.000 0.080 3 72447740 upstream gene variant G/A;C;T snv 2
rs2286742
HABP2
1.000 0.080 10 113580733 intron variant G/A;C snv 0.57; 8.2E-06 2
rs2336219
CD3EAP ; ERCC1
1.000 0.080 19 45409148 missense variant G/A snv 0.21 0.19 2
rs33954691
TERT
1.000 0.080 5 1255405 synonymous variant G/A snv 0.13 9.0E-02 2
rs367722824
PDGFRA
1.000 0.120 4 54278512 missense variant G/A snv 8.0E-06 2.1E-05 2
rs3740530
HABP2
1.000 0.080 10 113574365 synonymous variant C/T snv 0.63 0.55 2
rs3804329
ATG5
1.000 0.080 6 106238552 intron variant A/G snv 0.15 2