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: rs229526
rs229526
C1QTNF6
1 1.000 0.120 22 37185382 missense variant G/C;T snv 0.19; 4.0E-06 0.700 1.000 1 2011 2011