Variant (rsID / SNP)

rs151178822

rs151178822 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HSPG2. Location: chromosome 1, position 22,178,355. Clinical significance in the table: Uncertain significance.

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Reference-table entries

HSPG2Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 1:22178355
Cytoband: 1p36.12
HGVS: NM_005529.7(HSPG2):c.6935G>A (p.Arg2312Gln)
Allele change: Missense_R2312Q

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.