Variants & Targets

Analyze genetic variants with VEP prediction scores

Search Variant

Enter a variant marker in the format: chromosome_position_ref/alt

Format: chromosome_position_reference/alternate (e.g., 9_133445803_C/T)

Example Variants

9_133445803_C/T

ABL1missense variant

22_42526694_G/A

CYP2D6missense variant

16_31096368_G/A

VKORC1intron variant

10_96541616_C/T

CYP2C9missense variant

About VEP Scores

Variant Effect Predictor (VEP) scores help predict the functional impact of genetic variants. This tool aggregates predictions from 40+ algorithms to provide a consensus view of pathogenicity.

Pathogenic

Variant likely causes disease

Uncertain

Insufficient evidence

Benign

Variant not disease-causing