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: rs886041020
rs886041020
1 1.000 0.120 19 6495336 missense variant A/G snv 0.700 1.000 1 2014 2014
dbSNP: rs886041021
rs886041021
1 1.000 0.120 19 6495327 missense variant C/A;T snv 0.700 1.000 1 2014 2014
dbSNP: rs886041022
rs886041022
1 1.000 0.120 19 6495318 missense variant A/C snv 0.700 1.000 1 2015 2015