Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.44 (A)
Location

Chromosome 1:53593704 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59337212, rs1769311

This variation has 3 HGVS names - click the plus to show

Variation displays