官方服务：
资源简介：
SNPs from Dataset 1 in PLINK format.
应用场景：
创建时间：
2017-01-01
相关数据集
Table_4_Genotype–Phenotype Analysis of RPGR Variations: Reporting of 62 Chinese Families and a Literature Review.XLSX
PurposeRPGR is the most common cause of X-linked retinitis pigmentosa (RP), of which female carriers are also frequently affected. The aim of the current study was to explore the RPGR variation spectr
NIAID Data Ecosystem50
Table_1_Genotype-Phenotype Correlations in Charcot-Marie-Tooth Disease Due to MTMR2 Mutations and Implications in Membrane Trafficking.XLSX
Charcot-Marie-Tooth type 4 (CMT4) is an autosomal recessive severe form of neuropathy with genetic heterogeneity. CMT4B1 is caused by mutations in the myotubularin-related 2 (MTMR2) gene and as a memb
NIAID Data Ecosystem40
Detailed information for all individuals with CNV deletions in YBX1 or YBX3 included in Fig 4 and accompanying DECIPHER phenotypic data.
Detailed information for all individuals with CNV deletions in YBX1 or YBX3 included in Fig 4 and accompanying DECIPHER phenotypic data.
NIAID Data Ecosystem20
imputed-seq-genotypes-Chr19.33010000-34010000.vcf
Imputed genotypes for variants within 1Mbp of the Chr19:33.51 LC QTL, for 357 animals.
DataONE2017-12-15 更新40
Statistical evaluation on the genotype and allele frequency distribution.
Statistical evaluation on the genotype and allele frequency distribution.
NIAID Data Ecosystem20
