Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.17 (G)
Location

Chromosome 16:46684812 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs59393238

HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 14 transcripts and has 2579 sample genotypes.

Variant displays