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: rs351855
rs351855
FGFR4
58 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 0.020 1.000 2 2006 2015
dbSNP: rs1477349434
rs1477349434
ERBB2
1 1.000 17 39715520 missense variant G/C snv 4.0E-06 0.010 1.000 1 2006 2006
dbSNP: rs749491856
rs749491856
VEGFA
1 1.000 6 43782071 missense variant A/C snv 0.010 1.000 1 2010 2010