rs610932
This variant is located in the MS4A6A gene.
▶Research that mentions this SNP (2)
▶The prevalence of CD33 and MS4A6A variant in Chinese Han population with Alzheimer’s diseaseAssociationN=383Yu-Lei Deng et al.(2012)· Human Genetics
A case-control study of 190 AD patients and 193 controls in the Chinese Han population found that the T allele of rs3865444 in CD33 (OR=0.480, p<0.001) and the C allele of rs610932 in MS4A6A (OR=0.622, p=0.001) are associated with increased Alzheimer's disease risk, confirming previous GWAS findings in a non-Caucasian population.
▶A Comprehensive Genetic Association Study of Alzheimer Disease in African AmericansAssociationN=1,009Logue MW et al.(2011)· Archives of Neurology
This comprehensive genome-wide association study examined genetic variants contributing to late-onset Alzheimer's disease (AD) in 513 African American cases and 496 controls, plus replication in 5 white cohorts. The APOE ε4 allele showed strong association (P=9.69×10⁻²³), and after adjusting for APOE, rs6859 in PVRL2 remained significantly associated (P=0.0087). The study found associations with variants in CLU, PICALM, BIN1, EPHA1, MS4A, ABCA7, and CD33, though effect directions sometimes differed from white populations. Novel associations with suggestive evidence were identified in PROX1, CNTNAP2, STK24, and other genes, though not replicated in whites.
About MS4A6A
This gene encodes a member of the membrane-spanning 4A gene family. Members of this nascent protein family are characterized by common structural features and similar intron/exon splice boundaries and display unique expression patterns among hematopoietic cells and nonlymphoid tissues. The gene encoding this protein is localized to 11q12.1, among a cluster of family members. Alternative splicing of this gene results in several transcript variants that encode different protein isoforms. [provided by RefSeq, Oct 2011]
View all MS4A6A variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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