Variant (rsID / SNP)

rs36047130

rs36047130 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PPP1R17. Location: chromosome 7, position 31,732,084. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

PPP1R17Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 7:31732084
Cytoband: 7p14.3
HGVS: NM_006658.5(PPP1R17):c.29T>G (p.Leu10Arg)
Allele change: Missense_L10R

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.