Variant (rsID / SNP)

rs76153148

rs76153148 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CD2AP. Location: chromosome 6, position 47,544,734. Clinical significance in the table: Benign.

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Reference-table entries

CD2APBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 6:47544734
Cytoband: 6p12.3
HGVS: NM_012120.3(CD2AP):c.809-11C>A
Allele change: Silent

Associated conditions / phenotypes

Focal segmental glomerulosclerosis 3, susceptibility to

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.