RS1566734 PTPRJ

Health Risk Chr 11:48123822 snv missense variant

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What This Variant Does

"NOTE: the OMIM entry cited below refers to a somatic mutation, not a germline SNP PTPRJ haplotypes a...

Associated Conditions

Carcinoma of colon

Colorectal cancer

PTPRJ-related disorder

Carcinoma of colon

Colorectal cancer

PTPRJ-related disorder

Population Frequencies

gnomAD ALL

16.5%

1kG AFR

10.5%

1kG ALL

81%

1kG AMR

12.4%

1kG EAS

31.8%

1kG EUR

83.9%

1kG SAS

24.8%

Other Variants in PTPRJ