Variant (rsID / SNP)

rs900171

rs900171 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LRIG1. Location: chromosome 3, position 66,433,676. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

LRIG1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:66433676
Cytoband: 3p14.1
HGVS: NM_015541.3(LRIG1):c.2221T>C (p.Leu741=)
Allele change: Synonymous_L741L

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.