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variant

rs7975232

rs7975232 · 5 retained evidence mentions

Supporting evidence

TypeEntitySource evidenceConfidenceExtractor
variantrs7975232“Association of vitamin D receptor gene polymorphisms ApaI (rs7975232) and BsmI (rs1544410) with hepatocellular carcinoma susceptibility in Egyptian patients.”0.90hgvs_regex_v1
variantrs7975232“The aim of this study is to investigate the possible association of two identified mutations ApaI (rs7975232) and TaqI (rs731236).”0.90hgvs_regex_v1
variantrs7975232“RESULTS: For the ApaI single-nucleotide polymorphism (SNP) (rs7975232), only the heterozygous (Aa) genotype increased the risk of CRC (OR = 3.4, RR = 2.3, and P < 0.0001), whereas the TaqI SNP (rs731236) carriers with either the heterozygous (Tt) or homozygous (tt) genotype displayed an increased risk for the disease (OR = 6.18, RR = 4, P < 0.0001; OR = 3, RR = 2.4, P = 0.02, respectively).”0.90hgvs_regex_v1
variantrs7975232“Protective Association of Single Nucleotide Polymorphisms rs1861868-FTO and rs7975232-VDR and Obesity in Saudi Females.”0.90hgvs_regex_v1
variantrs7975232“Vitamin D Receptor ApaI (rs7975232) Polymorphism Confers Decreased Risk of Pulmonary Tuberculosis in Overall and African Population, but not in Asians: Evidence from a Meta-analysis.”0.90hgvs_regex_v1