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: rs6959584
rs6959584
1 1.000 0.080 7 106036059 3 prime UTR variant C/T snv 0.12 0.700 1.000 1 2016 2016
dbSNP: rs6967330
rs6967330
8 0.827 0.120 7 106018005 missense variant G/A snv 0.19 0.21 0.060 1.000 6 2015 2020
dbSNP: rs408223
rs408223
2 1.000 0.080 7 106021578 intron variant C/G snv 0.27 0.010 1.000 1 2020 2020