Variant (rsID / SNP)

rs10069050

rs10069050 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LYSMD3. Location: chromosome 5, position 89,820,984. The table records no clinical significance for this variant.

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Reference-table entries

LYSMD3Not classified

Variant type: synonymous_variant
Chromosome / position: 5:89820984
HGVS: NM_198273.2,c.123A>G,p.Glu41Glu
Allele change: Synonymous_E41E

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.