HaploReg

Explores functional annotations of the noncoding genome at specific haplotype blocks.

What it does

Essential for determining which specific candidate regulatory SNV within a large haplotype block is the true disease-causing variant.

STRC usage

Not yet tested on E1659A.

Connections

• STRC Variant c.4976A>C — Misha [see-also]
• STRC Gene [about]
• [part-of] Tools index