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Variant (rsID / SNP)

rs12990449

LRP1B

rs12990449 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LRP1B. Location: chromosome 2, position 142,567,910. The table records no clinical significance for this variant.

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Reference-table entries

LRP1BNot classified
Variant type
missense_variant
Chromosome / position
2:142567910
HGVS
NM_018557.3,c.143A>G,p.Gln48Arg
Allele change
Missense_Q48R

Public references

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