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: rs9398171
rs9398171
2 1.000 0.040 6 108662324 intron variant C/T snv 0.55 0.700 1.000 3 2015 2019
dbSNP: rs4945816
rs4945816
2 1.000 0.040 6 108680839 3 prime UTR variant C/T snv 0.53 0.700 1.000 1 2019 2019