Gene: UGT2B26P ×
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: rs13140844
rs13140844
UGT2B26P
1 4 69042989 intron variant A/T snv 0.67 0.700 1.000 1 2012 2012
dbSNP: rs4305590
rs4305590
UGT2B26P
1 4 69029013 intron variant A/C;T snv 0.700 1.000 1 2012 2012