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: rs397509428
rs397509428
ESR1
1 1.000 6 152011684 missense variant G/T snv 0.800 1.000 2 2013 2017
dbSNP: rs1131692059
rs1131692059
ESR1
1 1.000 6 152011740 missense variant G/A snv 0.800 0
dbSNP: rs104893956
rs104893956
ESR1
1 1.000 6 151842613 stop gained C/T snv 0.700 0
dbSNP: rs1562787582
rs1562787582
ESR1
1 1.000 6 152099207 3 prime UTR variant T/A snv 0.700 0
dbSNP: rs2046210
rs2046210 		21 0.708 0.280 6 151627231 intergenic variant G/A snv 0.41 0.700 0
dbSNP: rs6929137
rs6929137
CCDC170 ; LOC107986528
6 0.851 0.160 6 151615542 missense variant G/A snv 0.31 0.36 0.700 0
dbSNP: rs776119905
rs776119905
TMEM59
1 1.000 1 54032127 3 prime UTR variant C/A;G;T snv 4.1E-06; 4.1E-06 0.700 0