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: rs1516725
rs1516725
8 0.925 0.120 3 186106215 intron variant T/C snv 0.86 0.700 1.000 7 2013 2019
dbSNP: rs73052033
rs73052033
1 3 186110676 intron variant T/C snv 0.15 0.700 1.000 1 2019 2019
dbSNP: rs7647305
rs7647305
8 1.000 0.080 3 186116501 intron variant T/C snv 0.74 0.700 1.000 5 2009 2019
dbSNP: rs9816226
rs9816226
5 1.000 0.080 3 186116710 intron variant A/T snv 0.82 0.700 1.000 3 2010 2019