Variant (rsID / SNP)

rs201916993

rs201916993 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LRP5. Location: chromosome 11, position 68,177,526. Clinical significance in the table: Uncertain significance.

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Reference-table entries

LRP5Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 11:68177526
Cytoband: 11q13.2
HGVS: NM_002335.4(LRP5):c.2236C>T (p.Arg746Trp)
Allele change: Missense_R746W

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.