Variant (rsID / SNP)

rs3789044

rs3789044 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LRRN2. Location: chromosome 1, position 204,589,101. The table records no clinical significance for this variant.

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Reference-table entries

LRRN2Not classified

Variant type: missense_variant
Chromosome / position: 1:204589101
HGVS: NM_006338.3,c.20C>T,p.Pro7Leu
Allele change: Missense_P7L

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.