Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.41 (A)
Location

Chromosome 7:2577005 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

7:g.2577005G>A

Variation displays