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: rs1752911
rs1752911 		1 1.000 0.080 13 85777273 intron variant A/G snv 0.010 1.000 1 2014 2014
dbSNP: rs2981579
rs2981579
FGFR2
8 0.776 0.280 10 121577821 intron variant A/G snv 0.53 0.010 1.000 1 2014 2014
dbSNP: rs6678914
rs6678914
LGR6
3 0.882 0.080 1 202218048 intron variant G/A snv 0.37 0.010 1.000 1 2014 2014
dbSNP: rs889312
rs889312 		14 0.732 0.360 5 56736057 regulatory region variant C/A snv 0.69 0.010 1.000 1 2014 2014