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: rs11639372
rs11639372
5 0.925 0.080 15 78674313 intron variant C/T snv 0.30 0.700 1.000 1 2017 2017
dbSNP: rs6495309
rs6495309
10 0.807 0.080 15 78622903 upstream gene variant C/A;T snv 0.040 1.000 4 2009 2014
dbSNP: rs11072768
rs11072768
4 0.882 0.080 15 78637136 intron variant T/C;G snv 0.010 1.000 1 2016 2016
dbSNP: rs1948
rs1948
5 0.827 0.160 15 78625057 synonymous variant A/G;T snv 0.69 0.010 1.000 1 2018 2018
dbSNP: rs7178270
rs7178270
3 0.882 0.080 15 78628735 intron variant C/G;T snv 0.010 1.000 1 2010 2010