Gene: CYP19A1 ×
Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs727479
rs727479
CYP19A1 ; MIR4713 ; MIR4713HG
10 0.790 0.240 15 51242350 intron variant C/A;T snv 0.020 1.000 2 2009 2016
dbSNP: rs10046
rs10046
CYP19A1 ; MIR4713HG
18 0.708 0.400 15 51210789 3 prime UTR variant G/A snv 0.45 0.43 0.010 1.000 1 2012 2012
dbSNP: rs1065779
rs1065779
CYP19A1 ; MIR4713HG
3 0.882 0.120 15 51212614 intron variant A/C;T snv 0.43 0.010 1.000 1 2007 2007
dbSNP: rs28566535
rs28566535
CYP19A1
4 0.851 0.120 15 51308944 intron variant A/C;G;T snv 0.010 1.000 1 2007 2007
dbSNP: rs4775936
rs4775936
CYP19A1 ; MIR4713HG
7 0.790 0.200 15 51243825 intron variant C/T snv 0.36 0.010 1.000 1 2012 2012
dbSNP: rs700519
rs700519
CYP19A1 ; MIR4713HG
11 0.752 0.280 15 51215771 missense variant G/A snv 7.6E-02 8.0E-02 0.010 1.000 1 2007 2007
dbSNP: rs749292
rs749292
CYP19A1 ; MIR4713HG
4 0.851 0.160 15 51266534 intron variant G/A snv 0.44 0.010 1.000 1 2009 2009
dbSNP: rs752760
rs752760
CYP19A1
2 0.925 0.080 15 51339282 upstream gene variant C/T snv 0.57 0.010 1.000 1 2007 2007