Variant (rsID / SNP)

rs2306272

rs2306272 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LRIG1. Location: chromosome 3, position 66,434,643. 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: 3:66434643
Cytoband: 3p14.1
HGVS: NM_015541.3(LRIG1):c.1843A>G (p.Met615Val)
Allele change: Missense_M615V

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.