Variant (rsID / SNP)

rs1136287

rs1136287 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SERPINF1. Location: chromosome 17, position 1,673,276. Clinical significance in the table: Benign.

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Reference-table entries

SERPINF1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 17:1673276
Cytoband: 17p13.3
HGVS: NM_002615.7(SERPINF1):c.215C>T (p.Thr72Met)
Allele change: Missense_T72M

Associated conditions / phenotypes

Osteogenesis imperfecta type 6|Osteogenesis imperfecta

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.