首页/数据集/HGMD <i>SCN1A</i> mutation frequencies in patients and controls.

HGMD <i>SCN1A</i> mutation frequencies in patients and controls.

NIAID Data Ecosystem2026-03-09 收录

SCN1A基因突变频率

遗传病关联分析

数据链接：

https://figshare.com/articles/dataset/HGMD_i_SCN1A_i_mutation_frequencies_in_patients_and_controls_/3952694 数据链接链接失效反馈

官方服务：

资源简介：

HGMD SCN1A mutation frequencies in patients and controls.

应用场景：

创建时间：

2016-09-28

遗传病关联分析

罕见变异统计

The directory contains data described by Le Scouarnec et al. (2015) for the rare variant association analysis of Brugada syndrome (BrS). The quality control of this processed data is further detailed

NIAID Data Ecosystem50

年龄相关性黄斑变性

遗传病关联分析

Age-related Macular Degeneration (AMD) is a leading cause of incurable blindness in people over the age of 65. AMD is a late-onset multi-factorial neurodegenerative disease and its pathogenesis involv

NIAID Data Ecosystem50

The differences between groups with and without TB in genotypes and alleles frequencies of selected SNPs and results of odds ratio analysis in the overall participants.

遗传病关联分析

SNP等位基因频率比较

The differences between groups with and without TB in genotypes and alleles frequencies of selected SNPs and results of odds ratio analysis in the overall participants.

Figshare2024-05-09 更新30

Prader-Willi Syndrome Microbiota Targeted loci environmental. Prader-Willi Syndrome Microbiota

微生物组

遗传病关联分析

This study investigated the microbiome profiling (16S rRNA gene amplicons) of PWS individuals.

NIAID Data Ecosystem50

Variant frequencies and deleterious score predictions of carnitine acyltransferase genes.

基因变异功能预测

遗传病关联分析

Variant frequencies and deleterious score predictions of carnitine acyltransferase genes.

Figshare2016-10-31 更新30