Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.01 (A)
Location

Chromosome 2:208989998 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

2:g.208989998G>A

Variation displays