Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.17 (A)
Location

Chromosome 2:112829544 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms
HGVS name

2:g.112829544A>G

This variation has assays on 4 chips - click the plus to show

Variation displays