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: rs741301
rs741301
3 0.925 0.160 7 36878390 intron variant C/T snv 0.59 0.030 1.000 3 2013 2019
dbSNP: rs10951509
rs10951509
1 1.000 0.120 7 37173878 intron variant G/A;C snv 0.010 1.000 1 2013 2013
dbSNP: rs1345365
rs1345365
1 1.000 0.120 7 37161008 intron variant G/A snv 0.61 0.010 < 0.001 1 2019 2019
dbSNP: rs7782979
rs7782979
2 0.925 0.160 7 36865445 intron variant C/A snv 0.46 0.010 < 0.001 1 2019 2019