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: rs485499
rs485499
2 0.925 0.080 3 160028076 intron variant T/C snv 0.29 0.800 1.000 2 2011 2015
dbSNP: rs6441286
rs6441286
2 0.925 0.080 3 160011091 intron variant T/G snv 0.36 0.800 1.000 2 2009 2010
dbSNP: rs2366643
rs2366643
1 1.000 0.080 3 160018698 intron variant T/C;G snv 0.800 1.000 1 2012 2012
dbSNP: rs582537
rs582537
1 1.000 0.080 3 159992311 intron variant A/C;G snv 0.800 1.000 1 2012 2017
dbSNP: rs62270414
rs62270414
1 1.000 0.080 3 159921870 intron variant T/C snv 0.12 0.700 1.000 1 2012 2012
dbSNP: rs644587
rs644587
1 1.000 0.080 3 159945506 intron variant C/T snv 0.24 0.700 1.000 1 2017 2017
dbSNP: rs668998
rs668998
2 0.925 0.120 3 159997764 non coding transcript exon variant G/A snv 0.63 0.700 1.000 1 2012 2012
dbSNP: rs80014155
rs80014155
1 1.000 0.080 3 159907604 intron variant C/T snv 2.9E-03 0.700 1.000 1 2012 2012