Variant (rsID / SNP)

rs370363439

rs370363439 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRICKLE1. Location: chromosome 12, position 42,866,358. Clinical significance in the table: Likely benign.

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Reference-table entries

PRICKLE1Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 12:42866358
Cytoband: 12q12
HGVS: NM_153026.3(PRICKLE1):c.-40G>A
Allele change: Silent

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.