Variant (rsID / SNP)

rs666636

rs666636 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MT4. Location: chromosome 16, position 56,601,720. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

MT4Not classified

Variant type: missense_variant
Chromosome / position: 16:56601720
HGVS: NM_032935.3,c.89A>G,p.Tyr30Cys
Allele change: Missense_Y30C

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.