Original source

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

Alleles
C/G | Ancestral: G | Ambiguity code: S | MAF: 0.40 (G)
Location

Chromosome 1:109571989 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs1279339

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

Variation displays