Variant (rsID / SNP)

rs3742945

rs3742945 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TTC5. Location: chromosome 14, position 20,770,036. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

TTC5Not classified

Variant type: missense_variant
Chromosome / position: 14:20770036
HGVS: NM_138376.3,c.140A>G,p.Gln47Arg
Allele change: Missense_Q47R

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.