Variant (rsID / SNP)

rs11580409

rs11580409 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ERICH3. Location: chromosome 1, position 75,038,228. The table records no clinical significance for this variant.

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Reference-table entries

ERICH3Not classified

Variant type: missense_variant
Chromosome / position: 1:75038228
HGVS: NM_001002912.5,c.3166T>G,p.Leu1056Val
Allele change: Missense_L1056V

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.