Variant (rsID / SNP)

rs11588857

rs11588857 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LRRN2. Location: chromosome 1, position 204,587,047. The table records no clinical significance for this variant.

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Reference-table entries

LRRN2Not classified

Variant type: missense_variant
Chromosome / position: 1:204587047
HGVS: NM_006338.3,c.2074C>T,p.Pro692Ser
Allele change: Missense_P692S

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.