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: rs886037938
rs886037938
1 1.000 15 26621417 missense variant C/T snp 0.800 3 2013 2016
dbSNP: rs886037939
rs886037939
1 1.000 15 26580456 missense variant T/A snp 0.800 1 2016 2016
dbSNP: rs886037940
rs886037940
1 1.000 15 26567671 missense variant G/T snp 0.800 1 2016 2016
dbSNP: rs886037941
rs886037941
1 1.000 15 26561099 missense variant C/T snp 0.800 1 2016 2016
dbSNP: rs1057519549
rs1057519549
2 0.923 0.036 15 26567655 missense variant G/A snp 0.700 1 2017 2017
dbSNP: rs1057519550
rs1057519550
2 0.923 0.036 15 26621403 missense variant T/G snp 0.700 1 2017 2017