Variant (rsID / SNP)

rs2297792

rs2297792 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UBQLN4. Location: chromosome 1, position 156,011,444. Clinical significance in the table: Benign.

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Reference-table entries

UBQLN4Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:156011444
Cytoband: 1q22
HGVS: NM_020131.5(UBQLN4):c.1485A>G (p.Ile495Met)
Allele change: Missense_I475M

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.