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: rs2019960
rs2019960
2 0.925 0.160 8 128180025 intron variant T/C snv 0.27 0.800 1.000 3 2010 2014
dbSNP: rs2608053
rs2608053
1 1.000 0.120 8 128063586 intron variant T/C snv 0.50 0.800 1.000 1 2010 2010
dbSNP: rs13255292
rs13255292
2 0.925 0.120 8 128064327 intron variant C/T snv 0.24 0.700 1.000 1 2013 2013
dbSNP: rs2720680
rs2720680
4 0.851 0.160 8 128102971 intron variant A/G snv 0.33 0.700 1.000 1 2017 2017
dbSNP: rs4733809
rs4733809
1 1.000 0.120 8 127977046 intron variant C/T snv 0.54 0.700 1.000 1 2013 2013
dbSNP: rs752427
rs752427
1 1.000 0.120 8 127967762 intron variant C/T snv 0.55 0.700 1.000 1 2013 2013