rs13014982

Parent Gene: FIGN

Importance: 3
Less common allele: A = 30%
More common allele: G = 70%
My Genotype: Log In
Risk Allele:

Disease/Trait: Non-Small Cell Lung Carcinoma

rs13014982 is associated with Non-small Cell Lung Carcinoma (R) . It is reported to association with Platinum-induced myelosuppression in non-small cell lung cancer (variant homozygote model). No specific risk allele was identified in the study.

Disease/Trait: Response To Platinum Based Chemotherapy

rs13014982 is associated with Response To Platinum Based Chemotherapy (R) . It is reported to association with Platinum-induced myelosuppression in non-small cell lung cancer (variant homozygote model). No specific risk allele was identified in the study.

Disease/Trait: Myelosuppression

rs13014982 is associated with Myelosuppression (R) . It is reported to association with Platinum-induced myelosuppression in non-small cell lung cancer (variant homozygote model). No specific risk allele was identified in the study.