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: rs17305657
rs17305657
1 1.000 0.040 20 33218782 intron variant T/C snv 5.2E-02 0.700 1.000 2 2008 2011