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: 0.37 (T)
Location

Chromosome 17:63476833 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

17:g.63476833T>A

Variation displays