Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
T/- | Ancestral: T | MAF: 0.05 (T)
Location

Chromosome 4:73738833 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

4:g.73738833delT

Variation displays