Original source

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

Alleles
T/- | Ancestral: T | MAF: 0.06 (-)
Location

Chromosome 6:12715386 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs369798236

HGVS name

6:g.12715386delT

Variation displays