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: rs536403690
rs536403690
1 20 59161308 intron variant C/T snv 1.2E-03 0.700 1.000 1 2016 2016
dbSNP: rs558916355
rs558916355
1 20 59133359 intron variant C/T snv 2.7E-03 0.700 1.000 1 2016 2016
dbSNP: rs574551002
rs574551002
1 20 59210114 intron variant A/G snv 8.7E-04 0.700 1.000 1 2016 2016