Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.40 (G)
Location

Chromosome 16:80996163 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59304495

This variation has 23 HGVS names - click the plus to show

About this variant

This variant overlaps 23 transcripts and has 2511 individual genotypes.

Variation displays