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: rs1062980
rs1062980
4 0.827 0.080 15 78500185 3 prime UTR variant T/C snv 0.39 0.710 1.000 1 2009 2017
dbSNP: rs13180
rs13180
4 0.851 0.160 15 78497146 synonymous variant C/T snv 0.54 0.51 0.700 1.000 3 2008 2012
dbSNP: rs10519198
rs10519198
2 0.925 0.080 15 78450412 intron variant C/A;G snv 0.700 1.000 1 2012 2012
dbSNP: rs2656069
rs2656069
3 0.882 0.080 15 78453365 intron variant C/G;T snv 0.700 1.000 1 2012 2012