Variant (rsID / SNP)

rs1046268

rs1046268 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TJP3, APBA3. Location: chromosome 19, position 3,750,615. The table records no clinical significance for this variant.

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Reference-table entries

TJP3Not classified

Variant type: missense_variant
Chromosome / position: 19:3750615
HGVS: NM_001267561.2,c.2720T>C,p.Met907Thr
Allele change: Missense_M898T

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.