Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.08 (G)
Location

Chromosome 1:115830461 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs3730214, rs61346559

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

Variation displays