Gene: CYLD ×
Source: GWASDB ×
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: rs2302759
rs2302759
CYLD ; LOC105371251
1 1.000 0.040 16 50793690 intron variant A/C;G snv 4.0E-06; 0.79 0.700 1.000 1 2007 2007
dbSNP: rs3135503
rs3135503
CYLD
1 1.000 0.040 16 50757339 intron variant T/G snv 0.32 0.700 1.000 1 2007 2007
dbSNP: rs6500331
rs6500331
CYLD
1 1.000 0.040 16 50774815 intron variant G/A snv 0.51 0.700 1.000 1 2007 2007
dbSNP: rs7342715
rs7342715
CYLD
1 1.000 0.040 16 50753572 intron variant A/G snv 0.59 0.700 1.000 1 2007 2007
dbSNP: rs751919
rs751919
CYLD ; MIR3181 ; LOC102724907
1 1.000 0.040 16 50741834 intron variant T/G snv 0.35 0.700 1.000 1 2007 2007
dbSNP: rs8060598
rs8060598
CYLD
1 1.000 0.040 16 50747891 intron variant T/C snv 0.36 0.700 1.000 1 2007 2007
dbSNP: rs8062540
rs8062540
CYLD ; LOC105371251
1 1.000 0.040 16 50784021 non coding transcript exon variant A/G snv 0.39 0.700 1.000 1 2007 2007