Variant (rsID / SNP)

rs1064491

rs1064491 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PSG1. Location: chromosome 19, position 43,372,386. The table records no clinical significance for this variant.

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Reference-table entries

PSG1Not classified

Variant type: synonymous_variant
Chromosome / position: 19:43372386
HGVS: NM_001297773.2,c.1110A>G,p.Glu370Glu
Allele change: Synonymous_E277E

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.