Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10035432
C5orf46
1.000 0.040 5 147855193 upstream gene variant G/A snv 0.18 1
rs10054105
STARD4-AS1
0.925 0.080 5 111573636 intron variant T/G snv 0.17 3
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs103294 0.827 0.200 19 54293995 downstream gene variant T/C snv 0.82 7
rs1034866440
AR
0.851 0.160 X 67643401 missense variant G/A snv 5.7E-06 4
rs1045531
PSCA
0.882 0.080 8 142682129 synonymous variant C/A snv 0.45 0.44 3
rs10459953
NOS2
0.925 0.080 17 27800492 5 prime UTR variant C/A;G;T snv 3
rs1047100
FGFR2
1.000 0.040 10 121538644 synonymous variant T/A;C snv 1.2E-05; 0.78 1
rs1057519912
MED12
0.776 0.200 X 71129408 missense variant C/G;T snv 11
rs10786938 1.000 0.040 10 106280012 intergenic variant G/C;T snv 1
rs10983755 0.790 0.320 9 117702392 upstream gene variant G/A snv 3.2E-02 7
rs11084596 1.000 0.040 19 31614073 regulatory region variant T/C snv 0.35 3
rs11199879 1.000 0.040 10 121285698 regulatory region variant T/C snv 0.18 3
rs1126647
CXCL8
0.827 0.160 4 73743328 3 prime UTR variant A/T snv 0.31 8
rs1136201
ERBB2
0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 34
rs115336889
ROPN1L
1.000 0.040 5 10454257 intron variant G/A;C snv 1
rs11651052
HNF1B
0.851 0.200 17 37742390 intron variant G/A snv 0.50 7
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs12470143
SRD5A2
0.925 0.080 2 31538488 intron variant C/T snv 0.42 2
rs12621278
ITGA6
0.790 0.280 2 172446825 intron variant A/G snv 4.9E-02 7
rs12653946
CTD-2194D22.4
0.882 0.080 5 1895715 intron variant C/T snv 0.43 5
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs137852569
AR
0.752 0.320 X 67686030 missense variant G/A snv 9.4E-06 10
rs141179786 1.000 0.040 18 53662174 intergenic variant A/G;T snv 2.2E-02 1
rs148678804 1.000 0.040 10 22138360 intergenic variant G/A;T snv 2