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: rs12127701
rs12127701
4 1 109295642 intron variant A/G snv 6.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs17645031
rs17645031
3 1 109292316 downstream gene variant C/T snv 7.9E-02 0.700 1.000 1 2012 2012
dbSNP: rs41306199
rs41306199
3 1 109292541 3 prime UTR variant C/T snv 7.8E-02 0.700 1.000 1 2012 2012
dbSNP: rs413582
rs413582
3 1 109308504 upstream gene variant C/T snv 0.37 0.700 1.000 1 2012 2012
dbSNP: rs629001
rs629001
3 1 109296296 missense variant C/G;T snv 0.93 0.700 1.000 1 2012 2012