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: rs878854416
rs878854416
1 1.000 2 196242162 missense variant C/T snv 0.800 1.000 1 2017 2017
dbSNP: rs878854417
rs878854417
1 1.000 2 196225800 missense variant G/A snv 0.800 1.000 1 2017 2017
dbSNP: rs878854422
rs878854422
1 1.000 2 196242157 missense variant A/C snv 0.800 1.000 1 2017 2017
dbSNP: rs878854424
rs878854424
1 1.000 2 196220113 missense variant T/C snv 0.700 1.000 1 2017 2017