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: rs10859871
rs10859871 		2 1.000 0.040 12 95318100 intron variant A/C snv 0.37 0.010 1.000 1 2015 2015
dbSNP: rs1250248
rs1250248
FN1
4 1.000 0.040 2 215422370 intron variant A/G snv 0.77 0.010 1.000 1 2013 2013
dbSNP: rs17694933
rs17694933 		3 1.000 0.040 9 22164310 intergenic variant G/A snv 0.50 0.010 1.000 1 2015 2015
dbSNP: rs4141819
rs4141819
LOC105374786
2 1.000 0.040 2 67637543 intron variant C/T snv 0.71 0.010 1.000 1 2015 2015
dbSNP: rs7521902
rs7521902
LOC105376850
4 1.000 0.040 1 22164231 intergenic variant C/A snv 0.22 0.010 1.000 1 2013 2013