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Variant (rsID / SNP)

rs1744760

MROH8

rs1744760 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MROH8. Location: chromosome 20, position 35,740,794. The table records no clinical significance for this variant.

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Reference-table entries

MROH8Not classified
Variant type
missense_variant
Chromosome / position
20:35740794
HGVS
NM_152503.7,c.2747A>G,p.Gln916Arg
Allele change
Synonymous_P916P

Public references

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