Source: GWASCAT ×
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: rs134871
rs134871
1 22 42256710 intron variant T/C snv 0.44 0.700 1.000 1 2018 2018
dbSNP: rs4822112
rs4822112
1 22 42335534 intron variant G/T snv 0.88 0.700 1.000 1 2018 2018
dbSNP: rs5758659
rs5758659
1 22 42225997 intron variant C/T snv 0.34 0.700 1.000 1 2015 2015