Variant (rsID / SNP)

rs1697965

rs1697965 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TPPP. Location: chromosome 5, position 668,791. The table records no clinical significance for this variant.

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Reference-table entries

TPPPNot classified

Variant type: intron_variant
Chromosome / position: 5:668791
HGVS: NM_007030.3,c.312-2553G>A
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.