rs2984613

Parent Gene: PMF1, PMF1-BGLAP

Importance: 3
Less common allele: T = 31%
More common allele: C = 69%
My Genotype: Log In
Risk Allele: C, C

Disease/Trait: Intracerebral Hemorrhage

The C allele of rs2984613 is reported to be associated with Intracerebral Hemorrhage (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Intracerebral hemorrhage (nonlobar).

Disease/Trait: White Matter Hyperintensity Measurement

The C allele of rs2984613 is reported to be associated with White Matter Hyperintensity Measurement (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with White matter hyperintensity burden.