Variant (rsID / SNP)

rs1655519

rs1655519 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MROH7. Location: chromosome 1, position 55,119,515. The table records no clinical significance for this variant.

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Reference-table entries

MROH7Not classified

Variant type: missense_variant
Chromosome / position: 1:55119515
HGVS: NM_001039464.4,c.916T>G,p.Tyr306Asp
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.