Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.12 (G)
Location

Chromosome 16:109213 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs798609, rs57570743

This variation has 11 HGVS names - click the plus to show

Variation displays