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Variant (rsID / SNP)

rs62621241

MROH8

rs62621241 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MROH8. Location: chromosome 20, position 35,796,541. The table records no clinical significance for this variant.

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Reference-table entries

MROH8Not classified
Variant type
missense_variant
Chromosome / position
20:35796541
HGVS
NM_152503.7,c.631A>G,p.Ile211Val
Allele change
Missense_H211R

Public references

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