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Variant (rsID / SNP)

rs2075117

UNC80

rs2075117 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UNC80. Location: chromosome 2, position 210,843,383. The table records no clinical significance for this variant.

Reference-table entries

UNC80Not classified
Variant type
synonymous_variant
Chromosome / position
2:210843383
HGVS
NM_001371986.1,c.9069G>A,p.Gln3023Gln
Allele change
Synonymous_Q2957Q

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.