Variant (rsID / SNP)

rs1027392

rs1027392 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to USP29. Location: chromosome 19, position 57,641,146. The table records no clinical significance for this variant.

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Reference-table entries

USP29Not classified

Variant type: missense_variant
Chromosome / position: 19:57641146
HGVS: NM_001389643.1,c.1103A>G,p.Asn368Ser
Allele change: Missense_N368S

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.