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Variant (rsID / SNP)

rs3096380

CMTR2

rs3096380 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CMTR2. Location: chromosome 16, position 71,319,646. The table records no clinical significance for this variant.

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Reference-table entries

CMTR2Not classified
Variant type
missense_variant
Chromosome / position
16:71319646
HGVS
NM_001099642.2,c.178C>T,p.Leu60Phe
Allele change
Missense_L60F

Associated conditions / phenotypes

Missense_L60F

Public references

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