Variant (rsID / SNP)

rs41275442

rs41275442 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MACROD2. Location: chromosome 20, position 15,967,390. The table records no clinical significance for this variant.

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Reference-table entries

MACROD2Not classified

Variant type: missense_variant
Chromosome / position: 20:15967390
HGVS: NM_001351661.2,c.1004C>T,p.Thr335Met
Allele change: Missense_T335M

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.