Variant (rsID / SNP)

rs666647

rs666647 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MT4. Location: chromosome 16, position 56,601,722. 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: 16:56601722
HGVS: NM_032935.3,c.91T>C,p.Trp31Arg
Allele change: Missense_W31R

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.