Variant (rsID / SNP)

rs3745746

rs3745746 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CABP5. Location: chromosome 19, position 48,537,585. The table records no clinical significance for this variant.

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Reference-table entries

CABP5Not classified

Variant type: missense_variant
Chromosome / position: 19:48537585
HGVS: NM_019855.5,c.383T>C,p.Val128Ala
Allele change: Missense_V128A

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.