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: rs16897515
rs16897515
1 1.000 0.040 6 27310241 missense variant C/A snv 0.13 0.18 0.800 1.000 2 2009 2013
dbSNP: rs7746199
rs7746199
1 1.000 0.040 6 27293545 intron variant C/T snv 0.18 0.800 1.000 1 2009 2017
dbSNP: rs3800316
rs3800316
1 1.000 0.040 6 27288323 intron variant A/C snv 0.33 0.700 1.000 2 2009 2011
dbSNP: rs3800318
rs3800318
1 1.000 0.040 6 27295862 intron variant A/T snv 0.18 0.700 1.000 1 2009 2009