Variant (rsID / SNP)

rs1147504

rs1147504 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PTPRZ1. Location: chromosome 7, position 121,653,398. The table records no clinical significance for this variant.

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Reference-table entries

PTPRZ1Not classified

Variant type: missense_variant
Chromosome / position: 7:121653398
HGVS: NM_002851.3,c.4298G>A,p.Gly1433Asp
Allele change: Missense_G1433D

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.