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: rs2144908
rs2144908
5 0.851 0.120 20 44357077 intron variant G/A snv 0.18 0.100 1.000 10 2006 2019
dbSNP: rs6103716
rs6103716
1 1.000 0.080 20 44370990 intron variant A/C snv 0.37 0.700 1.000 1 2019 2019
dbSNP: rs2425637
rs2425637
3 0.925 0.080 20 44395409 intron variant G/T snv 0.42 0.010 < 0.001 1 2010 2010
dbSNP: rs3212183
rs3212183
2 0.925 0.080 20 44406498 intron variant C/T snv 0.58 0.030 0.667 3 2005 2017
dbSNP: rs2425640
rs2425640
1 1.000 0.080 20 44399397 intron variant A/G snv 0.63 0.010 1.000 1 2004 2004
dbSNP: rs6031558
rs6031558
1 1.000 0.080 20 44371003 intron variant C/G snv 0.76 0.010 1.000 1 2005 2005