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Variant (rsID / SNP)

rs55676538

MTCL1

rs55676538 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MTCL1. Location: chromosome 18, position 8,819,246. The table records no clinical significance for this variant.

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Reference-table entries

MTCL1Not classified
Variant type
missense_variant
Chromosome / position
18:8819246
HGVS
NM_001395333.1,c.4225C>T,p.Arg1409Cys
Allele change
Missense_R1049C

Public references

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