Variant (rsID / SNP)

rs112996909

rs112996909 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MROH1. Location: chromosome 8, position 145,266,722. The table records no clinical significance for this variant.

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Reference-table entries

MROH1Not classified

Variant type: intron_variant
Chromosome / position: 8:145266722
HGVS: NM_032450.3,c.1142-8781A>G
Allele change: Silent

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.