Original source

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

Alleles
T/A | Ancestral: A | Ambiguity code: W | MAF: 0.12 (A)
Location

Chromosome 17:7080816 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms
HGVS name

17:g.7080816T>A

Variation displays