Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs1012891

TMX4

rs1012891 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMX4. Location: chromosome 20, position 7,980,390. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

TMX4Not classified
Variant type
synonymous_variant
Chromosome / position
20:7980390
HGVS
NM_021156.4,c.456G>A,p.Pro152Pro
Allele change
Synonymous_P152P

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.