Variant (rsID / SNP)

rs6451173

rs6451173 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TTC23L. Location: chromosome 5, position 34,840,841. The table records no clinical significance for this variant.

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Reference-table entries

TTC23LNot classified

Variant type: missense_variant
Chromosome / position: 5:34840841
HGVS: NM_001386170.1,c.65A>G,p.His22Arg
Allele change: Missense_H22R

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.