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Variant (rsID / SNP)

rs3749010

LRP1B

rs3749010 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LRP1B. Location: chromosome 2, position 141,571,329. The table records no clinical significance for this variant.

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Reference-table entries

LRP1BNot classified
Variant type
synonymous_variant
Chromosome / position
2:141571329
HGVS
NM_018557.3,c.5256A>G,p.Ser1752Ser
Allele change
Synonymous_S1752S

Public references

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