Variant (rsID / SNP)

rs12199003

rs12199003 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GFRAL. Location: chromosome 6, position 55,196,587. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

GFRALNot classified

Variant type: missense_variant
Chromosome / position: 6:55196587
HGVS: NM_207410.2,c.97C>T,p.Arg33Cys
Allele change: Missense_R33C

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.