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: rs1051730
rs1051730
43 0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 0.700 1.000 4 2008 2010
dbSNP: rs12914385
rs12914385
18 0.790 0.160 15 78606381 intron variant C/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs138544659
rs138544659
5 1.000 0.040 15 78608359 intron variant T/G snv 0.28 0.700 1.000 1 2017 2017