Gene: USP49 ×
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: rs11964516
rs11964516
USP49
1 6 41892514 intron variant T/C snv 0.17 0.700 1.000 1 2018 2018
dbSNP: rs12661667
rs12661667
USP49
5 6 41824807 intron variant C/T snv 0.20 0.700 1.000 1 2012 2012
dbSNP: rs2395792
rs2395792
USP49
1 6 41884449 intron variant T/G snv 0.97 0.700 1.000 1 2016 2016
dbSNP: rs6899876
rs6899876
USP49
3 6 41829232 intron variant T/C;G snv 0.23 0.700 1.000 1 2012 2012
dbSNP: rs7753507
rs7753507
USP49
3 6 41816356 intron variant C/T snv 0.52 0.700 1.000 1 2012 2012