Variant (rsID / SNP)

rs6793110

rs6793110 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LRIG1. Location: chromosome 3, position 66,444,615. Clinical significance in the table: Benign.

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Reference-table entries

LRIG1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:66444615
Cytoband: 3p14.1
HGVS: NM_015541.3(LRIG1):c.1317C>T (p.Ser439=)
Allele change: Synonymous_S439S

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.