Original source

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

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

Chromosome 7:39016981 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

7:g.39016981T>A

Variation displays