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: rs17064520
rs17064520
1 1.000 0.080 18 58242398 intron variant C/T snv 0.19 0.700 1.000 1 2000 2000