Original source

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

Alleles
G/C | Ambiguity code: S
Location

Chromosome 6:10399922 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs2857056

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

Variation displays