Variant (rsID / SNP)

rs3734676

rs3734676 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PDSS2. Location: chromosome 6, position 107,780,479. Clinical significance in the table: Benign.

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Reference-table entries

PDSS2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 6:107780479
Cytoband: 6q21
HGVS: NM_020381.4(PDSS2):c.11G>C (p.Arg4Pro)
Allele change: Missense_R4P

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.