Variant (rsID / SNP)

rs3744549

rs3744549 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLSCR3, TNK1. Location: chromosome 17, position 7,293,715. The table records no clinical significance for this variant.

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Reference-table entries

PLSCR3Not classified

Variant type: missense_variant
Chromosome / position: 17:7293715
HGVS: NM_001201576.2,c.877G>A,p.Val293Ile
Allele change: Missense_V293I

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.