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Variant (rsID / SNP)

rs7167612

TRIP4

rs7167612 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRIP4. Location: chromosome 15, position 64,737,225. The table records no clinical significance for this variant.

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Reference-table entries

TRIP4Not classified
Variant type
synonymous_variant
Chromosome / position
15:64737225
HGVS
NM_016213.5,c.1596G>A,p.Glu532Glu
Allele change
Synonymous_E532E

Public references

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