rs2298948

Parent Gene: GCFC2

Importance: 3
Less common allele: C = 26%
More common allele: T = 74%
My Genotype: Log In
Risk Allele: C

Disease/Trait: Hippocampal Atrophy

The C allele of rs2298948 is reported to be associated with Hippocampal Atrophy (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Hippocampal atrophy (Hippocampal volume).