Variant (rsID / SNP)

rs41266007

rs41266007 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HSPG2. Location: chromosome 1, position 22,169,325. Clinical significance in the table: Benign.

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Reference-table entries

HSPG2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:22169325
Cytoband: 1p36.12
HGVS: NM_005529.7(HSPG2):c.8848G>A (p.Gly2950Arg)
Allele change: Missense_G2950R

Associated conditions / phenotypes

Lethal Kniest-like syndrome|Schwartz-Jampel syndrome|Connective tissue disorder

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.