owencqueen/cgbench_data huggingface dataset:
Gene: SCN1A (HGNC:10585)
Evidence Code: PVS1 — Very Strong
Modification Type: Disease-specific,General recommendation
Follow SVI guidance per workflow in Tayoun et al (2018), included as “PVS1 Decision Tree”.
Gene: SCN1A (HGNC:10585)
Evidence Code: PVS1 — Strong
Modification Type: Disease-specific,General recommendation
Follow SVI guidance per workflow in Tayoun et al (2018), included as “PVS1 Decision Tree”.
Gene: SCN1A (HGNC:10585)
Evidence Code: PVS1 — Moderate
Modification Type: Disease-specific,General recommendation
Follow SVI guidance per workflow in Tayoun et al (2018), included as “PVS1 Decision Tree”.
Gene: SCN1A (HGNC:10585)
Evidence Code: PVS1 — Supporting
Modification Type: Disease-specific,General recommendation
Follow SVI guidance per workflow in Tayoun et al (2018), included as “PVS1 Decision Tree”.