Variant (rsID / SNP)

rs73981411

rs73981411 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TTC19. Location: chromosome 17, position 15,929,933. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

TTC19Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 17:15929933
Cytoband: 17p12
HGVS: NM_017775.4(TTC19):c.911G>C (p.Arg304Thr)
Allele change: Missense_R197T

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.