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: rs11636753
rs11636753
4 0.882 0.120 15 78636604 intron variant G/T snv 0.35 0.020 1.000 2 2012 2015
dbSNP: rs1948
rs1948
5 0.827 0.160 15 78625057 synonymous variant A/G;T snv 0.69 0.020 1.000 2 2017 2018
dbSNP: rs3813567
rs3813567
2 1.000 0.080 15 78642209 intron variant G/A snv 0.77 0.010 1.000 1 2010 2010
dbSNP: rs4887074
rs4887074
2 1.000 0.080 15 78659768 intron variant G/C snv 0.56 0.010 1.000 1 2018 2018