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Variant (rsID / SNP)

rs9369265

TREML4

rs9369265 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TREML4. Location: chromosome 6, position 41,196,605. The table records no clinical significance for this variant.

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Reference-table entries

TREML4Not classified
Variant type
missense_variant
Chromosome / position
6:41196605
HGVS
NM_198153.3,c.217T>C,p.Trp73Arg
Allele change
Missense_W73R

Public references

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