rs2284932

Parent Gene: KLF7

Importance: 3
Less common allele: A = 35%
More common allele: G = 65%
My Genotype: Log In
Risk Allele: C

Disease/Trait: Salivary Gland Lesion

The C allele of rs2284932 is reported to be associated with Salivary Gland Lesion (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Lachrymal/Salivary gland lesion in type 1 autoimmune pancreatitis.

Disease/Trait: Autoimmune Pancreatitis Type 1

The C allele of rs2284932 is reported to be associated with Autoimmune Pancreatitis Type 1 (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Lachrymal/Salivary gland lesion in type 1 autoimmune pancreatitis.

Disease/Trait: Lachrymal Gland Lesion

The C allele of rs2284932 is reported to be associated with Lachrymal Gland Lesion (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Lachrymal/Salivary gland lesion in type 1 autoimmune pancreatitis.