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: rs121434569
rs121434569
EGFR ; EGFR-AS1
70 0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 0.010 < 0.001 1 2011 2011
dbSNP: rs3760396
rs3760396
CCL2
13 0.732 0.280 17 34254422 upstream gene variant G/C snv 0.15 0.010 < 0.001 1 2016 2016
dbSNP: rs766779326
rs766779326
ESR1
2 1.000 0.040 6 151944344 missense variant C/T snv 4.0E-06 7.0E-06 0.010 1.000 1 2019 2019