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: rs780094
rs780094
27 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.740 1.000 4 2010 2016
dbSNP: rs1260326
rs1260326
21 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.010 1.000 1 2011 2011
dbSNP: rs780092
rs780092
4 0.827 0.160 2 27520287 intron variant A/G snv 0.18 0.010 1.000 1 2016 2016