Variant (rsID / SNP)

rs34577247

rs34577247 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LRP1. Location: chromosome 12, position 57,578,673. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

LRP1Not classified

Variant type: missense_variant
Chromosome / position: 12:57578673
HGVS: NM_002332.3,c.6238G>A,p.Asp2080Asn
Allele change: Missense_D2080N

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.