Variant (rsID / SNP)

rs35760408

rs35760408 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMCO4. Location: chromosome 1, position 20,072,082. The table records no clinical significance for this variant.

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Reference-table entries

TMCO4Not classified

Variant type: missense_variant
Chromosome / position: 1:20072082
HGVS: NM_001349112.3,c.820G>A,p.Gly274Ser
Allele change: Missense_G274S

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.