Source: BEFREE ×
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: rs6010620
rs6010620
19 0.701 0.360 20 63678486 intron variant A/C;G snv 0.900 0.952 16 2009 2020
dbSNP: rs2297440
rs2297440
9 0.763 0.080 20 63680946 intron variant T/C snv 0.81 0.820 1.000 2 2009 2018
dbSNP: rs115303435
rs115303435
1 1.000 0.040 20 63694806 missense variant G/A snv 3.2E-03 1.1E-03 0.010 1.000 1 2018 2018
dbSNP: rs6062302
rs6062302
1 0.882 0.040 20 63689615 synonymous variant T/C snv 0.74 0.81 0.010 1.000 1 2018 2018