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Six individuals were heterozygote carriers of the CSRP3 p.W4R variant and two carried the MYH6 p.A1004S variant.
Among the 28 PTC samples, 24 are classic PTC, one tall cell variant and two follicular variant of PTC.
Three potentially functional BANK1 SNPs (including a splice branch point-site variant and two coding variants) are associated with SLE.
The distance between each pair of variants was calculated and networks were created for each patient, where each node is a variant and two nodes are connected by a link if the nucleotide distance between them is 1.
All students were living in the Netherlands at the time of the study although 2 students in the online variant and two students in the classroom-based variant came from other countries (Ukraine and Germany versus Canada and Germany, respectively).
Here, an association was found between the presence of a variant and two terms jointly - the 'Thrombocytopenia' and 'Increased Mean Platelet Volume' terms - while regression analysis is typically performed trait by trait in a univariate fashion.
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Multiple allelic variants of these proteins were identified, different allelic variants dominated in different continents; the observed variation was predicted to impact the antigenicity and structure of two SP0148 variants, one SP1912 variant and four SP2108 variants, however these variants were each only present in a small fraction of the global population (<2%).
DF, an organochemically synthesized linkage variant, and five major Phase I metabolites were covalently coupled to carrier proteins.
Five individuals were heterozygous carriers of the MYBPC3 p.variantandanthree three carried the MYH7 p.M982T variant.
We genotyped the GWAS common variant and four rare variants previously reported for ABCA7 in 3476 European Americans.
Whole-exome sequencing confirmed the subject's isozygosity for the LIFR variant and ten rare variants (Table S1).
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com