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Variant (rsID / SNP)

rs9508908

ZMYM5

rs9508908 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZMYM5. Location: chromosome 13, position 20,398,742. The table records no clinical significance for this variant.

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Reference-table entries

ZMYM5Not classified
Variant type
missense_variant
Chromosome / position
13:20398742
HGVS
NM_001142684.2,c.1885G>A,p.Val629Ile
Allele change
Missense_V629I

Public references

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