Do rare variant genotypes predict common variant genotypes?

BMC Proceedings

Table 1 Significant regressions for unrelated individuals

Rare or common variant type	N significant	N total	% significant
Nonsynonymous/nonsynonymous	89	298	29.5
Nonsynonymous/synonymous	74	397	21.3
Synonymous/nonsynonymous	77	282	27.3
Synonymous/synonymous	91	330	27.6

The number of nominally significant (P < 0.05) regressions of the CVGS and the SRVGS did not differ significantly according to functional type (synonymous vs. nonsynonymous) of rare or common variants.

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