Variant (rsID / SNP)

rs7535965

rs7535965 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRDM16. Location: chromosome 1, position 3,313,282. Clinical significance in the table: Benign.

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Reference-table entries

PRDM16Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:3313282
Cytoband: 1p36.32
HGVS: NM_022114.4(PRDM16):c.676+125G>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.