Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.47 (G)

Chromosome 16:89792600 (forward strand) | View in location tab

Most severe consequence
Non coding transcript exon variant
Evidence status


Archive dbSNP rs74251563, rs17232546

HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 7 transcripts and has 2600 sample genotypes.

Variant displays