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Variant (rsID / SNP)

rs61745766

LRP11

rs61745766 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LRP11. Location: chromosome 6, position 150,174,278. The table records no clinical significance for this variant.

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Reference-table entries

LRP11Not classified
Variant type
missense_variant
Chromosome / position
6:150174278
HGVS
NM_032832.6,c.632T>G,p.Leu211Arg
Allele change
Missense_L211R

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.