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: rs2630765
rs2630765
2 5 177449824 intron variant T/C snv 0.50 0.700 1.000 1 2013 2013
dbSNP: rs2731662
rs2731662
1 5 177445493 intron variant A/G snv 0.50 0.700 1.000 1 2013 2013
dbSNP: rs335434
rs335434
1 5 177440275 intron variant T/C snv 0.43 0.700 1.000 1 2013 2013
dbSNP: rs335435
rs335435
1 5 177440942 synonymous variant A/G snv 0.45 0.46 0.700 1.000 1 2013 2013
dbSNP: rs466256
rs466256
1 5 177448955 intron variant C/A snv 0.47 0.700 1.000 1 2013 2013