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: rs1514175
rs1514175
4 1.000 0.080 1 74525960 intron variant A/G snv 0.48 0.700 1.000 3 2010 2013
dbSNP: rs113313252
rs113313252
2 1 74534327 intron variant -/T delins 0.700 1.000 1 2013 2013
dbSNP: rs12142020
rs12142020
2 1 74534327 intron variant A/T snv 0.50 0.700 1.000 1 2013 2013
dbSNP: rs201167096
rs201167096
2 1 74534327 intron variant -/T delins 0.700 1.000 1 2013 2013