Source: BEFREE ×
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: rs4471514
rs4471514
VEZT
1 1.000 0.120 12 95273561 intron variant C/T snv 0.48 0.010 1.000 1 2012 2012
dbSNP: rs6060373
rs6060373
UQCC1
2 0.925 0.200 20 35326405 intron variant A/G snv 0.49 0.010 1.000 1 2011 2011
dbSNP: rs745738344
rs745738344
TNF
28 0.653 0.600 6 31576786 synonymous variant G/A snv 1.6E-05 1.4E-05 0.010 1.000 1 2007 2007
dbSNP: rs7568069
rs7568069
ZNF638
1 1.000 0.120 2 71357355 intron variant G/A snv 0.48 0.010 1.000 1 2017 2017
dbSNP: rs8025374
rs8025374
CYP19A1 ; MIR4713HG
1 1.000 0.120 15 51226173 intron variant T/C;G snv 0.010 1.000 1 2012 2012