Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
A/T | Ancestral: A | Ambiguity code: W | MAF: < 0.01 (T)
Location

Chromosome 20:57224387 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

20:g.57224387A>T

Variation displays