Variant (rsID / SNP)

rs138974661

rs138974661 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNFSF11. Location: chromosome 13, position 43,155,281. Clinical significance in the table: Benign.

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Reference-table entries

TNFSF11Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 13:43155281
Cytoband: 13q14.11
HGVS: NM_003701.4(TNFSF11):c.239C>T (p.Ser80Leu)
Allele change: Missense_S7L

Associated conditions / phenotypes

Autosomal recessive osteopetrosis 2|Increased bone mineral density

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.