Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10046
MIR4713HG ; CYP19A1
0.708 0.400 15 51210789 3 prime UTR variant G/A snv 0.45 0.43 18
rs4646
MIR4713HG ; CYP19A1
0.716 0.360 15 51210647 3 prime UTR variant A/C snv 0.67 0.70 16
rs700518
CYP19A1 ; MIR4713HG
0.732 0.320 15 51236915 synonymous variant T/C snv 0.43 0.40 13
rs700519
MIR4713HG ; CYP19A1
0.752 0.280 15 51215771 missense variant G/A snv 7.6E-02 8.0E-02 11
rs1008805
MIR4713HG ; CYP19A1
0.851 0.160 15 51257402 intron variant G/A snv 0.64 7
rs4775936
MIR4713HG ; CYP19A1
0.790 0.200 15 51243825 intron variant C/T snv 0.36 7
rs28566535
CYP19A1
0.851 0.120 15 51308944 intron variant A/C;G;T snv 4
rs2236722
CYP19A1 ; MIR4713HG
0.851 0.120 15 51242798 missense variant A/G snv 3.4E-03 9.1E-04 4
rs7176005
CYP19A1
0.925 0.080 15 51339082 upstream gene variant C/T snv 0.21 3
rs3751591
CYP19A1 ; MIR7973-1 ; MIR7973-2
0.925 0.080 15 51314513 intron variant A/G snv 0.13 3
rs1413421847
MIR4713HG ; CYP19A1
0.882 0.160 15 51242801 missense variant C/T snv 2.8E-05 3
rs936306
MIR4713HG ; CYP19A1
0.925 0.080 15 51287401 intron variant C/T snv 0.30 3
rs730154
CYP19A1
0.925 0.080 15 51299007 intron variant T/C snv 0.30 2
rs11856927
CYP19A1 ; MIR4713HG
0.925 0.080 15 51256508 intron variant G/T snv 0.58 2
rs1004982
LOC112268146 ; CYP19A1
0.925 0.080 15 51321614 non coding transcript exon variant T/C;G snv 2
rs774053181
MIR4713HG ; CYP19A1
0.925 0.080 15 51242874 missense variant G/C snv 4.0E-06 2