Variant (rsID / SNP)

rs564117

rs564117 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAM187B. Location: chromosome 19, position 35,718,938. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

FAM187BNot classified

Variant type: missense_variant
Chromosome / position: 19:35718938
HGVS: NM_152481.2,c.646G>A,p.Val216Ile
Allele change: Missense_V216I

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.