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: rs11593576
rs11593576
1 0.925 0.040 10 79256139 intron variant C/T snv 0.29 0.800 1.000 1 2010 2010