Original source

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

G/C | Ancestral: C | Ambiguity code: S | MAF: 0.01 (G)

Chromosome 16:74748216 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs690326

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 2 transcripts and has 2512 sample genotypes.

Variant displays