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. Author manuscript; available in PMC: 2014 Nov 1.
Published in final edited form as: Clin Genet. 2012 Oct 10;84(5):496–500. doi: 10.1111/cge.12018

Table 2. Polyphen2 predictions of rare variants (MAF<1%) in NSCL/P candidate genes.

NSCL/P Only NSCL/P and 1kGP/ESP6500 1kGP/ESP6500 Only
No. % No. % No. %
Probably Damaging 14 45.2% 5 41.7% 318 39.7%
Possibly Damaging 7 22.6% 2 16.7% 119 14.8%
Benign 10 32.3% 5 41.7% 365 45.5%
Total 31 12 802