Original source

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

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

Chromosome 16:89768689 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs17233092, rs58404229

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and has 2594 sample genotypes.

Variant displays