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: rs16969968
rs16969968
37 0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 0.100 0.963 27 2008 2018
dbSNP: rs11637635
rs11637635
3 0.882 0.080 15 78584808 intron variant A/G snv 0.68 0.010 1.000 1 2010 2010
dbSNP: rs17408276
rs17408276
3 0.882 0.080 15 78589276 non coding transcript exon variant T/C snv 0.28 0.010 1.000 1 2010 2010
dbSNP: rs17486278
rs17486278
9 0.827 0.120 15 78575140 intron variant A/C snv 0.32 0.010 1.000 1 2010 2010
dbSNP: rs3829787
rs3829787
3 0.882 0.080 15 78563924 upstream gene variant C/T snv 0.27 0.010 1.000 1 2013 2013
dbSNP: rs481134
rs481134
3 0.882 0.080 15 78585221 intron variant A/G snv 0.64 0.010 1.000 1 2010 2010
dbSNP: rs503464
rs503464
6 0.851 0.080 15 78565554 5 prime UTR variant T/A snv 0.28 0.010 1.000 1 2013 2013
dbSNP: rs588765
rs588765
6 0.827 0.200 15 78573083 intron variant T/A;C snv 0.010 1.000 1 2015 2015
dbSNP: rs667282
rs667282
13 0.790 0.120 15 78571130 intron variant T/C snv 0.28 0.010 < 0.001 1 2013 2013