Variant (rsID / SNP)

rs738479

rs738479 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PARVB. Location: chromosome 22, position 44,489,896. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

PARVBNot classified

Variant type: splice_region_variant&synonymous_variant
Chromosome / position: 22:44489896
HGVS: NM_001003828.3,c.300T>C,p.Leu100Leu
Allele change: Synonymous_L100L

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.