Source: ALL
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: rs1297536872
rs1297536872
FUT8
1 1.000 14 65721948 missense variant C/G;T snv 0.700 0
dbSNP: rs1334593208
rs1334593208
FUT8
1 1.000 14 65721882 stop gained C/T snv 1.2E-05 0.700 0
dbSNP: rs1460811017
rs1460811017
FUT8
1 1.000 14 65669360 stop gained C/T snv 8.0E-06 0.700 0
dbSNP: rs1555388034
rs1555388034
FUT8
1 1.000 14 65724328 splice region variant G/T snv 0.700 0