Gene: SUGCT ×
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: rs4379368
rs4379368
SUGCT
3 0.925 0.040 7 40426601 intron variant C/T snv 0.12 0.830 1.000 4 2013 2019
dbSNP: rs186166891
rs186166891
SUGCT
1 7 40367277 intron variant A/C;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs61693171
rs61693171
SUGCT
1 7 40378133 intron variant G/- del 0.81 0.700 1.000 1 2016 2016