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: rs4038131
rs4038131
2 0.925 0.120 2 17593765 intron variant A/G snv 0.12 0.800 1.000 1 2012 2012
dbSNP: rs1033301
rs1033301
1 1.000 0.080 2 17592731 intron variant A/C snv 0.11 0.700 1.000 1 2012 2012
dbSNP: rs4038129
rs4038129
1 1.000 0.080 2 17593479 intron variant A/G snv 0.11 0.700 1.000 1 2012 2012