Variant (rsID / SNP)

rs1500481

rs1500481 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MROH2A. Location: chromosome 2, position 234,702,459. The table records no clinical significance for this variant.

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Reference-table entries

MROH2ANot classified

Variant type: missense_variant
Chromosome / position: 2:234702459
HGVS: NM_001367507.1,c.811T>C,p.Tyr271His
Allele change: Missense_Y271H

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.