Original source

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

Alleles
G/C | Ambiguity code: S | MAF: 0.48 (C)
Location

Chromosome 16:2895247 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57076052, rs3204700

This variation has 5 HGVS names - click the plus to show

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

Variation displays