Variant (rsID / SNP)

rs28439396

rs28439396 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MROH5. Location: chromosome 8, position 142,476,555. The table records no clinical significance for this variant.

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Reference-table entries

MROH5Not classified

Variant type: non_coding_transcript_exon_variant
Chromosome / position: 8:142476555
HGVS: NR_160399.1,n.2511T>C
Allele change: Missense_C811R

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.