Variant (rsID / SNP)

rs4417518

rs4417518 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMC3. Location: chromosome 15, position 81,624,768. The table records no clinical significance for this variant.

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Reference-table entries

TMC3Not classified

Variant type: missense_variant
Chromosome / position: 15:81624768
HGVS: NM_001080532.3,c.3295G>A,p.Asp1099Asn
Allele change: Silent

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.