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: rs11708067
rs11708067
5 0.882 0.080 3 123346931 intron variant A/G snv 0.19 0.800 1.000 1 2012 2012
dbSNP: rs12330631
rs12330631
1 3 123370987 intron variant C/T snv 0.26 0.700 1.000 1 2019 2019
dbSNP: rs2877716
rs2877716
3 3 123375604 intron variant T/C snv 0.76 0.700 1.000 1 2012 2012