Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.02 (A)
Location

Chromosome 16:46709752 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs1201301, rs688057

This variation has 4 HGVS names - click the plus to show

Variation displays