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: rs10046
rs10046
CYP19A1 ; MIR4713HG
18 0.708 0.400 15 51210789 3 prime UTR variant G/A snv 0.45 0.43 0.100 0.818 11 2008 2018
dbSNP: rs4646
rs4646
CYP19A1 ; MIR4713HG
16 0.716 0.360 15 51210647 3 prime UTR variant A/C snv 0.67 0.70 0.100 1.000 10 2008 2015
dbSNP: rs700519
rs700519
CYP19A1 ; MIR4713HG
11 0.752 0.280 15 51215771 missense variant G/A snv 7.6E-02 8.0E-02 0.070 0.714 7 2003 2016
dbSNP: rs2236722
rs2236722
CYP19A1 ; MIR4713HG
4 0.851 0.120 15 51242798 missense variant A/G snv 3.4E-03 9.1E-04 0.040 1.000 4 2002 2010
dbSNP: rs4775936
rs4775936
CYP19A1 ; MIR4713HG
7 0.790 0.200 15 51243825 intron variant C/T snv 0.36 0.030 0.667 3 2008 2019
dbSNP: rs700518
rs700518
CYP19A1 ; MIR4713HG
13 0.732 0.320 15 51236915 synonymous variant T/C snv 0.43 0.40 0.030 1.000 3 2014 2015
dbSNP: rs1008805
rs1008805
CYP19A1 ; MIR4713HG
7 0.851 0.160 15 51257402 intron variant G/A snv 0.64 0.020 1.000 2 2008 2017
dbSNP: rs1004982
rs1004982
CYP19A1 ; LOC112268146
2 0.925 0.080 15 51321614 non coding transcript exon variant T/C;G snv 0.010 1.000 1 2008 2008
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 2013 2013
dbSNP: rs11856927
rs11856927
CYP19A1 ; MIR4713HG
2 0.925 0.080 15 51256508 intron variant G/T snv 0.58 0.010 1.000 1 2014 2014
dbSNP: rs1413421847
rs1413421847
CYP19A1 ; MIR4713HG
3 0.882 0.160 15 51242801 missense variant C/T snv 2.8E-05 0.010 1.000 1 2009 2009
dbSNP: rs28566535
rs28566535
CYP19A1
4 0.851 0.120 15 51308944 intron variant A/C;G;T snv 0.010 1.000 1 2008 2008
dbSNP: rs3751591
rs3751591
CYP19A1 ; MIR7973-2 ; MIR7973-1
3 0.925 0.080 15 51314513 intron variant A/G snv 0.13 0.010 1.000 1 2016 2016
dbSNP: rs7176005
rs7176005
CYP19A1
3 0.925 0.080 15 51339082 upstream gene variant C/T snv 0.21 0.010 1.000 1 2019 2019
dbSNP: rs730154
rs730154
CYP19A1
2 0.925 0.080 15 51299007 intron variant T/C snv 0.30 0.010 < 0.001 1 2008 2008
dbSNP: rs774053181
rs774053181
CYP19A1 ; MIR4713HG
2 0.925 0.080 15 51242874 missense variant G/C snv 4.0E-06 0.010 1.000 1 2018 2018
dbSNP: rs936306
rs936306
CYP19A1 ; MIR4713HG
3 0.925 0.080 15 51287401 intron variant C/T snv 0.30 0.010 1.000 1 2008 2008