{{Rsnum
|rsid=707746
|Chromosome=19
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=PSG2
|position=43071794
|Gene_s=PSG2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}https://www.23andme.com/you/community/thread/14602/

http://www.cell.com/AJHG/retrieve/pii/S0002929712003576 {{doi|10.1016/j.ajhg.2012.07.002}} Exome Sequencing Identifies [[FUS]] Mutations as a Cause of Essential Tremor ... Functional considerations suggest that the pathogenic effects of ET-specific FUS mutations are different from the effects observed when FUS is mutated in amyotrophic lateral sclerosis cases; we have shown that the ET FUS nonsense mutation is degraded by the nonsense-mediated-decay pathway, whereas amyotrophic lateral sclerosis FUS mutant transcripts are not...

This snp was flagged as Suspect:  Variation suspected to be false positive due to artifacts of the presence of a paralogous sequence in the genome  (Musumeci et al. 2010) (Sudmant et al. 2010) or evidence suggested sequencing error or computation artifacts.