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Variant (rsID / SNP)

rs1503185

PTPRJ

rs1503185 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PTPRJ. Location: chromosome 11, position 48,146,622. The table records no clinical significance for this variant.

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Reference-table entries

PTPRJNot classified
Variant type
missense_variant
Chromosome / position
11:48146622
HGVS
NM_002843.4,c.977G>A,p.Arg326Gln
Allele change
Missense_R326Q

Associated conditions / phenotypes

Colorectal Cancer 1

Public references

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