Variant (rsID / SNP)

rs147419407

rs147419407 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TM4SF19. Location: chromosome 3, position 196,054,374. Clinical significance in the table: Uncertain significance.

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Reference-table entries

TM4SF19Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 3:196054374
Cytoband: 3q29
HGVS: NM_138461.4(TM4SF19):c.88G>C (p.Ala30Pro)
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.