Original source

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

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

Chromosome 4:74604550 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

4:g.74604550delT

Variation displays