Variant (rsID / SNP)

rs4732620

rs4732620 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NUGGC. Location: chromosome 8, position 27,925,204. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

NUGGCNot classified

Variant type: missense_variant
Chromosome / position: 8:27925204
HGVS: NM_001010906.2,c.538A>G,p.Ser180Gly
Allele change: Missense_S180G

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.