RS121909293 CTRC

Health Risk Chr 1:15445716 snv missense variant

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What This Variant Does

"[OMIM:?]

Associated Conditions

Pancreatitis

chronic

susceptibility to

Hereditary pancreatitis

Pancreatitis

chronic

susceptibility to

Hereditary pancreatitis

GWAS Studies (1)

Trait	Risk Allele	OR / Beta	P-value	Study
CTRC protein levels	T	OR: 0.64	6E-53	PubMed

Population Frequencies

gnomAD ALL

0.4%

1kG AFR

100%

1kG ALL

0.2%

1kG AMR

100%

1kG EAS

100%

1kG EUR

99.2%

1kG SAS

100%

Other Variants in CTRC