rs117070989

Parent Gene: OLIG3

Importance: 3
Less common allele: A = 0%
More common allele: C = 100%
My Genotype: Log In
Risk Allele: C, C

Disease/Trait: Cognitive Impairment

The C allele of rs117070989 is reported to be associated with Cognitive Impairment (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Cognitive decline rate in late mild cognitive impairment (EA).

Disease/Trait: Cognitive Decline Measurement

The C allele of rs117070989 is reported to be associated with Cognitive Decline Measurement (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Cognitive decline rate in late mild cognitive impairment (EA).

Disease/Trait: Cognitive Impairment

The C allele of rs117070989 is reported to be associated with Cognitive Impairment (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Cognitive decline rate in late mild cognitive impairment.

Disease/Trait: Cognitive Decline Measurement

The C allele of rs117070989 is reported to be associated with Cognitive Decline Measurement (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Cognitive decline rate in late mild cognitive impairment.