Variant (rsID / SNP)

rs7073610

rs7073610 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CWF19L1. Location: chromosome 10, position 102,006,625. Clinical significance in the table: Likely benign.

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Reference-table entries

CWF19L1Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 10:102006625
Cytoband: 10q24.31
HGVS: NM_018294.6(CWF19L1):c.776C>T (p.Pro259Leu)
Allele change: Missense_P122L

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.