Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.01 (T)
Location

Chromosome 1:145926584 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs4483357

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

This variation has assays on 5 chips - click the plus to show

Variation displays