Variant (rsID / SNP)

rs2748416

rs2748416 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MROH5. Location: chromosome 8, position 142,490,120. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

MROH5Not classified

Variant type: non_coding_transcript_exon_variant
Chromosome / position: 8:142490120
HGVS: NR_160399.1,n.945C>A
Allele change: Missense_L289M

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.