Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs759173

MROH2A

rs759173 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MROH2A. Location: chromosome 2, position 234,704,690. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

MROH2ANot classified
Variant type
splice_region_variant&synonymous_variant
Chromosome / position
2:234704690
HGVS
NM_001367507.1,c.1137T>C,p.Leu379Leu
Allele change
Synonymous_L382L

Public references

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