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: rs854560
rs854560
113 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.060 1.000 6 2010 2019
dbSNP: rs662
rs662
157 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.050 1.000 5 2012 2019
dbSNP: rs765657236
rs765657236
1 1.000 0.120 7 95318360 synonymous variant G/A snv 8.0E-06 0.020 1.000 2 2016 2018