Variant (rsID / SNP)

rs17588988

rs17588988 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRIM69. Location: chromosome 15, position 45,047,402. The table records no clinical significance for this variant.

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Reference-table entries

TRIM69Not classified

Variant type: missense_variant
Chromosome / position: 15:45047402
HGVS: NM_182985.5,c.311A>G,p.Lys104Arg
Allele change: Silent

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.