Variant (rsID / SNP)

rs61761332

rs61761332 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNFSF11. Location: chromosome 13, position 43,180,951. Clinical significance in the table: Uncertain significance.

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Reference-table entries

TNFSF11Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 13:43180951
Cytoband: 13q14.11
HGVS: NM_003701.4(TNFSF11):c.851G>A (p.Arg284Gln)
Allele change: Missense_R211Q

Associated conditions / phenotypes

Autosomal recessive osteopetrosis 2

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.