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: 0.39 (G)
Location

Chromosome 2:205797619 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs3184858, rs16837690

This variation has 2 HGVS names - click the plus to show

This variation has assays on 5 chips - click the plus to show

Variation displays