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: rs77924615
rs77924615
7 1.000 0.080 16 20381010 intron variant G/A snv 0.16 0.700 1.000 7 2016 2019
dbSNP: rs11864909
rs11864909
7 0.851 0.160 16 20389517 intron variant C/T snv 0.23 0.700 1.000 1 2018 2018
dbSNP: rs4494548
rs4494548
1 16 20360266 intron variant G/A snv 0.11 0.700 1.000 1 2019 2019