Because the previously identified nsSNPs having moderately significant p -values showed an obvious impact on osteoporosis-related phenotypes [ 12 , 35 – 42 ], some of our discovered nsSNPs were anticipated to be meaningful genetic variants involved in osteoporosis etiology.
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Association of the I264T variant in the sulfide quinone reductase-like (SQRDL) gene with osteoporosis in Korean postmenopausal women.
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