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Variant (rsID / SNP)

rs4515815

TMCO4

rs4515815 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMCO4. Location: chromosome 1, position 20,020,994. The table records no clinical significance for this variant.

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Reference-table entries

TMCO4Not classified
Variant type
missense_variant
Chromosome / position
1:20020994
HGVS
NM_001349112.3,c.1433G>A,p.Arg478His
Allele change
Missense_R478H

Public references

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