Original source

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

Alleles
T/- | Ancestral: T | MAF: 0.02 (-)
Location

Chromosome 20:938806 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

20:g.938806delT

Variation displays