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1 records shown · first 60Risk Y-haplotypes and pathogenic variants of Arab-ancestry boys with autism by an exome-wide association study.
PMID 32996047 | DOI 10.1007/s11033-020-05832-6 · Molecular biology reports · 2020 · 15 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| variant | rs13447352 | “Y-chromosome haplotyping analysis of 6 SNPs such as rs1865680, rs2032624, rs2032658, rs2032631, rs9786153 and rs13447352 uncovered the most significant protective (ACGACA p = 2.94 × 10-9) among the controls and the high risk Y-haplotype (GAAGTC p = 6.85 × 10-6) among autistic boys.” | 0.90 | hgvs_regex_v1 |
| gene | MCC | “Exome association study revealed 6 susceptible genes, MCC, AUTS2, VSX1, SETBP1, CNTN3, and PCDH11Y that were known for autistic disorder.” | 0.98 | hgnc_dict_v1 |
| gene | AUTS2 | “Exome association study revealed 6 susceptible genes, MCC, AUTS2, VSX1, SETBP1, CNTN3, and PCDH11Y that were known for autistic disorder.” | 0.98 | hgnc_dict_v1 |
| gene | VSX1 | “Exome association study revealed 6 susceptible genes, MCC, AUTS2, VSX1, SETBP1, CNTN3, and PCDH11Y that were known for autistic disorder.” | 0.98 | hgnc_dict_v1 |