Variant (rsID / SNP)

rs966384

rs966384 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LRG1. Location: chromosome 19, position 4,538,599. The table records no clinical significance for this variant.

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Reference-table entries

LRG1Not classified

Variant type: missense_variant
Chromosome / position: 19:4538599
HGVS: NM_052972.3,c.397C>T,p.Pro133Ser
Allele change: Missense_P133S

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.