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: rs7173743
rs7173743
2 0.851 0.120 15 78849442 intron variant T/C snv 0.45 0.800 1.000 1 2013 2018
dbSNP: rs11072811
rs11072811
1 1.000 0.040 15 78839988 intron variant A/C snv 0.51 0.700 1.000 1 2018 2018
dbSNP: rs11637783
rs11637783
1 1.000 0.040 15 78846658 intron variant T/C snv 0.34 0.700 1.000 1 2018 2018
dbSNP: rs4468572
rs4468572
1 1.000 0.040 15 78832133 intron variant T/C snv 0.58 0.700 1.000 1 2015 2015
dbSNP: rs6495335
rs6495335
1 1.000 0.040 15 78824791 intron variant G/T snv 0.63 0.700 1.000 1 2018 2018
dbSNP: rs7164479
rs7164479
1 1.000 0.040 15 78830712 intron variant C/T snv 0.58 0.700 1.000 1 2017 2017