Variant (rsID / SNP)

rs7188856

rs7188856 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NAGPA. Location: chromosome 16, position 5,075,633. Clinical significance in the table: Benign.

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Reference-table entries

NAGPABenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 16:5075633
Cytoband: 16p13.3
HGVS: NM_016256.4(NAGPA):c.1394C>T (p.Thr465Ile)
Allele change: Missense_T465I

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.