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: rs118203347
rs118203347
1 1.000 0.120 9 132927208 missense variant T/C snv 7.0E-06 0.700 0
dbSNP: rs118203385
rs118203385
1 1.000 0.120 9 132923383 missense variant A/C;G snv 0.700 0
dbSNP: rs1323541164
rs1323541164
1 1.000 0.120 9 132921834 missense variant A/C snv 0.700 0