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: rs1057519753
rs1057519753
9 0.763 0.120 1 64846664 missense variant C/A snv 0.700 1.000 2 2011 2011
dbSNP: rs11208534
rs11208534
1 1.000 0.040 1 64877383 intron variant A/G snv 0.16 0.700 1.000 1 2017 2017
dbSNP: rs310199
rs310199
1 1.000 0.040 1 64884439 intron variant A/G snv 0.43 0.700 1.000 1 2017 2017
dbSNP: rs310201
rs310201
1 1.000 0.040 1 64883925 intron variant A/G snv 0.37 0.700 1.000 1 2017 2017
dbSNP: rs310202
rs310202
1 1.000 0.040 1 64883861 intron variant A/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs3790541
rs3790541
1 1.000 0.040 1 64875884 3 prime UTR variant C/T snv 0.15 0.700 1.000 1 2017 2017