Variant (rsID / SNP)

rs704959

rs704959 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TTC21A. Location: chromosome 3, position 39,180,263. The table records no clinical significance for this variant.

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Reference-table entries

TTC21ANot classified

Variant type: missense_variant
Chromosome / position: 3:39180263
HGVS: NM_001366899.1,c.3950G>A,p.Arg1317Lys
Allele change: Missense_R1316K

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.