Original source

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

Alleles
T/A | Ambiguity code: W | MAF: 0.01 (A)
Location

Chromosome 6:29757807 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

6:g.29757807T>A

Variation displays