Variant (rsID / SNP)

rs61271372

rs61271372 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UNC80. Location: chromosome 2, position 210,858,145. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

UNC80Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 2:210858145
Cytoband: 2q34
HGVS: NM_001371986.1(UNC80):c.9503C>T (p.Pro3168Leu)
Allele change: Missense_P3102L

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.