Genetic variants identified in linkage region after removal of SNVs present in dbSNP with a MAF >2%.
收藏数据链接：
官方服务：
资源简介：
Chr: chromosome; Ref: reference base; Obs: observed base; NCBI RS: NCBI Reference Sequence; Variant Category: NS SNV = nonsynonymous single nucleotide variant, S SNV = synonymous single nucleotide variant; Note: NC = Not confirmed by Sanger sequencing, C = Confirmed by Sanger sequencing, E = excluded.
创建时间：
2015-12-02
