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: rs11122330
rs11122330
1 1.000 0.040 1 231762845 intron variant A/G snv 0.14 0.010 1.000 1 2013 2013
dbSNP: rs1538979
rs1538979
3 0.882 0.160 1 231761122 intron variant C/T snv 0.19 0.010 1.000 1 2013 2013
dbSNP: rs6675281
rs6675281
7 0.827 0.080 1 231818355 missense variant C/T snv 0.11 0.14 0.010 1.000 1 2013 2013