Original source

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

Alleles
G/C | Ancestral: C | Ambiguity code: S | MAF: 0.01 (G)
Location

Chromosome 2:208249074 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57877504

This variation has 12 HGVS names - click the plus to show

Variation displays