Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs2372675

MREG

rs2372675 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MREG. Location: chromosome 2, position 216,825,842. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

MREGNot classified
Variant type
missense_variant
Chromosome / position
2:216825842
HGVS
NM_001372188.1,c.395G>A,p.Arg132His
Allele change
Silent

Public references

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