Variant (rsID / SNP)

rs886044356

rs886044356 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CRPPA. Location: chromosome 7, position 16,445,959. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

CRPPAConflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 7:16445959
Cytoband: 7p21.2
HGVS: NM_001101426.4(CRPPA):c.261A>G (p.Val87=)
Allele change: Synonymous_V87V

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.