Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W | MAF: 0.10 (A)
Location

Chromosome 7:39016598 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

7:g.39016598T>A

Variation displays