Variant (rsID / SNP)

rs142285781

rs142285781 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UBR1. Location: chromosome 15, position 43,299,402. Clinical significance in the table: Uncertain significance.

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Reference-table entries

UBR1Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 15:43299402
Cytoband: 15q15.2
HGVS: NM_174916.3(UBR1):c.3290C>T (p.Thr1097Met)
Allele change: Missense_T1097M

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.