Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs726016

MROH2A

rs726016 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MROH2A. Location: chromosome 2, position 234,725,502. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

MROH2ANot classified
Variant type
missense_variant
Chromosome / position
2:234725502
HGVS
NM_001367507.1,c.2932T>C,p.Trp978Arg
Allele change
Missense_W981R

Public references

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