Variant (rsID / SNP)

rs35069201

rs35069201 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UBR1. Location: chromosome 15, position 43,317,071. Clinical significance in the table: Benign.

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Reference-table entries

UBR1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 15:43317071
Cytoband: 15q15.2
HGVS: NM_174916.3(UBR1):c.2695A>G (p.Ile899Val)
Allele change: Missense_I899V

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.