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Results 1 - 10 of 23 for SNP 2
  1. NLRP1 gene 
    ... Guimaraes R, Segat L, Araujo J, Crovella S. Two SNPs in NLRP3 gene are involved in the predisposition ...
    https://medlineplus.gov/genetics/gene/nlrp1 - Genetics
  2. GeneReviews Glossary From the National Institutes of Health (National Center for Biotechnology Information)  
    Genetic Testing/Reference Desk ... Genetic Testing ... Newborn Screening/Reference Desk ... Newborn Screening ... National Center for Biotechnology Information ... From the National ...
    https://www.ncbi.nlm.nih.gov/books/NBK5191 - External Health Links
  3. Is hair color determined by genetics?: MedlinePlus Genetics 
    ... E, Bartosz G, Strapagiel D. Association of five SNPs with human hair colour in the Polish population. Homo. 2017 Mar;68(2):134-144. doi: 10.1016/j.jchb.2017. ...
    https://medlineplus.gov/genetics/understanding/traits/haircolor - Genetics
  4. ATG16L1 gene 
    ... S. A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1. Nat Genet. 2007 Feb;39(2):207-11. doi: 10.1038/ng1954. Epub 2006 ...
    https://medlineplus.gov/genetics/gene/atg16l1 - Genetics
  5. Kawasaki disease 
    ... of the C Allele of the ITPKC Gene SNP rs28493229 in Kawasaki Disease: Association With Disease Susceptibility and BCG Scar Reactivation. Pediatr Infect Dis J. 2011 Feb;30(2):148-52. doi: 10.1097/INF.0b013e3181f43a4e. Citation ...
    https://medlineplus.gov/genetics/condition/kawasaki-disease - Genetics
  6. ITPKC gene 
    ... of the C Allele of the ITPKC Gene SNP rs28493229 in Kawasaki Disease: Association With Disease Susceptibility and BCG Scar Reactivation. Pediatr Infect Dis J. 2011 Feb;30(2):148-52. doi: 10.1097/INF.0b013e3181f43a4e. Citation ...
    https://medlineplus.gov/genetics/gene/itpkc - Genetics
  7. STRC gene 
    ... Sagi M, Rehm HL, Krantz ID. Genome-wide SNP genotyping identifies the Stereocilin (STRC) gene as a major contributor to pediatric bilateral sensorineural hearing impairment. Am J Med Genet A. 2012 Feb;158A(2):298-308. doi: 10.1002/ajmg.a.34391. ...
    https://medlineplus.gov/genetics/gene/strc - Genetics
  8. Thrombocytopenia-absent radius syndrome 
    ... C. Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome. Nat Genet. 2012 Feb 26;44(4):435-9, S1-2. doi: 10.1038/ng.1083. Citation on PubMed ...
    https://medlineplus.gov/.../thrombocytopenia-absent-radius-syndrome - Genetics
  9. Chromosome 1 
    ... C. Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome. Nat Genet. 2012 Feb 26;44(4):435-9, S1-2. doi: 10.1038/ng.1083. Citation on PubMed ...
    https://medlineplus.gov/genetics/chromosome/1 - Genetics
  10. RBM8A gene 
    ... C. Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome. Nat Genet. 2012 Feb 26;44(4):435-9, S1-2. doi: 10.1038/ng.1083. Citation on PubMed ...
    https://medlineplus.gov/genetics/gene/rbm8a - Genetics
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