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Variant (rsID / SNP)

rs6431631

MROH2A

rs6431631 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MROH2A. Location: chromosome 2, position 234,688,036. The table records no clinical significance for this variant.

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Reference-table entries

MROH2ANot classified
Variant type
missense_variant
Chromosome / position
2:234688036
HGVS
NM_001367507.1,c.32C>A,p.Ala11Asp
Allele change
Missense_A11D

Public references

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