Gene: CYP19A1 ×
Source: INFERRED ×
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: rs10519302
rs10519302
CYP19A1
1 15 51307486 intron variant A/G snv 0.20 0.700 1.000 2 2015 2019
dbSNP: rs16964211
rs16964211
CYP19A1 ; MIR4713HG
2 15 51238298 intron variant G/A snv 0.14 0.700 1.000 2 2010 2014
dbSNP: rs2305707
rs2305707
CYP19A1 ; MIR4713HG
2 15 51277213 non coding transcript exon variant A/G;T snv 0.25 0.700 1.000 2 2010 2019
dbSNP: rs146939415
rs146939415
CYP19A1 ; MIR4713HG
1 15 51230013 intron variant G/C snv 8.7E-03 0.700 1.000 1 2019 2019
dbSNP: rs2445752
rs2445752
CYP19A1 ; MIR4713HG
2 15 51284188 intron variant A/G snv 0.30 0.700 1.000 1 2019 2019
dbSNP: rs28757157
rs28757157
CYP19A1 ; MIR4713HG
1 15 51253204 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs3751599
rs3751599
CYP19A1 ; MIR4713HG
2 15 51281336 intron variant G/A snv 2.3E-03 0.700 1.000 1 2013 2013