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Variant (rsID / SNP)

rs3093983

MCCD1

rs3093983 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MCCD1. Location: chromosome 6, position 31,496,925. The table records no clinical significance for this variant.

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Reference-table entries

MCCD1Not classified
Variant type
missense_variant
Chromosome / position
6:31496925
HGVS
NM_001011700.3,c.134G>A,p.Ser45Asn
Allele change
Missense_S45N

Public references

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