Variant (rsID / SNP)

rs41303893

rs41303893 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMCO4. Location: chromosome 1, position 20,066,380. The table records no clinical significance for this variant.

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Reference-table entries

TMCO4Not classified

Variant type: synonymous_variant
Chromosome / position: 1:20066380
HGVS: NM_001349112.3,c.1116G>T,p.Val372Val
Allele change: Synonymous_V372V

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.